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Durchschnittliches Gehaltsniveau in den letzten 12 Monaten: "Clinical Research Associate in "

Währung: EUR USD Jahr: 2020
Das Balkendiagramm zeigt die Änderung des Gehaltsniveaus in der Clinical Research Associate Branche in

Verteilung des Stellenangebots "Clinical Research Associate" in

Währung: EUR
Das Balkendiagramm zeigt die Änderung des Gehaltsniveaus in der Clinical Research Associate Branche in

Empfohlene Stellenangebote

Assistant Professor
Medizinische Universität Wien, Wien
Within the Medical Department of Clinical Pharmacology at the Medical University of Vienna a position as Assistant Professor Translational Pharmacology and Pharmacometrics according to § 99 (5) University Law 2002 (UG) is announced. The Medical University of Vienna is one of Europe’s premiere institutions for biomedical and clinical research. We are looking for a highly qualified scientist in the fields of translational pharmacology and pharmacometrics with a special focus on population pharmacokinetic modelling and pharmacokineticpharmacodynamic models with enthusiasm for inter- and multidisciplinary research, and commitment to teaching. The candidate is expected to have outstanding expertise in pharmacometrics and its associated fields to strengthen, expand and cross-link existing research cluster topics within the university (https://www.meduniwien.ac.at/web/forschung/forschungsschwerpunkte/). Your profile: • Completed scientific or medical education with PhD or equivalent degree. • International recognition in the respective research area. • Successful and continuous acquisition of peer-reviewed and industry third-party funding. • Educational and didactic qualifications including supervision of Masters and PhD students. • Diversity and gender competence. • International working experience. We offer: The successful candidate will be offered an Assistant Professor position for a maximum duration of six years. Should the candidate meet the conditions stipulated in the qualification agreement, she/he will be promoted to tenured Associate Professor. Conditions and criteria are defined in the official career track guidelines of the university (Career scheme for the scientific University staff according to Section 99 (5) Universities Act 2002 “New qualification agreement”). The gross salary for this position is based on the collective agreement for university employees (§49, A2) and may be adjusted depending on previous work experience. We provide an excellent research environment including high-end core research facilities as well as targeted PhD programs. The MedUni Vienna aims to increase the proportion of women in executive positions and encourages qualified female candidates to apply. In case of equivalent qualifications, preference will be given to female applicants. The MedUni Vienna has child care facilities on campus. Please submit your application in English to faculty-recruitingmeduniwien.ac.at by June 15th, 2021 at the latest. All files should be merged into a single PDF. Applications should include: • list of publications • summary of research and teaching activities • a concept of future research plans including how these could contribute to interlink and strengthen the research cluster • up to five key publications with the possibility of electronic downloading • three letters of reference • contact details of three referees Applicants are also requested to complete the application form (FactSheet) posted online and to attach it to their application (https://www.meduniwien.ac.at/Factsheet_Professuren_99_5_UG). Information in accordance with the General Data Protection Regulation can be found at About us The Medical University of Vienna is one of the most established medical training and research institutions in Europe. With 8,000 students, it is today the largest medical training facility in the German-speaking area. Together, 26 university departments and three clinical institutes as well as twelve basic science centres and numerous highly specialized laboratories make the Medical University of Vienna one of the most important cutting-edge research institutions in biomedicine.
Studienmanager / Clinical Research Associate (m/w/d)
St. Anna Kinderkrebsforschung, Wien
Hoppla Etwas ist schiefgelaufen. Bitte informieren Sie uns darüber, dass Sie auf dieser Seite gelandet sind, indem Sie eine E Mail an unseren Customer Service schicken (infojob.at). Kopieren Sie bitte diese Seite und senden Sie uns diese ausgefüllt zu. Ihre URL ist: https://www.job.at/stellenangeboteStudienmanager-Clinical-Research-Associate-m-w-d-Wien-St-Anna-Kinderkrebsforschung562907-inline.html?cidPartner_job___at Ihre IP ist: 191.96.255.38 Ihre Browserdetails sind: Mozilla/5.0 (Windows NT 10.0; Win64; x64) AppleWebKit/537.36 (KHTML, like Gecko) Chrome/75.0.3741.0 Safari/537.36 Datum: Fri Apr 16 2021 14:23:44 GMT0000 (UTC)
Country Trial Operations Lead
Novartis Group, Wien
Für ein spannendes Unternehmen suchen wir einen geeigneten Kandidaten zur Besetzung dieser Position. Lead local the Clinical Trial Associates (CTAs) team to ensure fast and good quality submission of initial clinical trial applications and subsequent updates to Health Authority (HA) and Ethics Committee (EC) Oversees the Country Trial Monitoring budget process and ensure appropriate controls are in place to deliver on Country Trial Monitoring business objectives Ensures the timeliness, accuracy and quality of Trial Master File (TMF) documents, including study activation and ongoing TMF maintenance in prep for TMF inspection readiness Is responsible for resource management of the CTA team and including the assessment and allocation of country resources to ensure a balanced workload across the team Manages and addresses Country Trial Monitoring performance targets per defined Trial Monitoring objectives, and serves as an escalation for study start up, drug supply, finance and business analytics management Ensures adherence to financial standards, prevailing legislation, GCP, Ethical Committee and SOP requirements University degree in life sciences (e.g. chemistry, biology, biotechnology or similar) Minimum of 5 years’ experience working in clinical research operations planning & execution Strong people management and team leadership skills Excellent knowledge of all aspects of clinical drug development with particular emphasis on trial execution and monitoring Thorough understanding of the international aspects of drug development process, including expert knowledge of international standards Strong capability in working in a country matrixed environment Fluency in English and strong interpersonal, negotiation and conflict resolution skills
Project Associate
United Nations Industrial Development Organization, Wien
Project Specialist (Value Chain Development) Vacancy Announcement VACANCY ANNOUNCEMENT TEMPORARY APPOINTMENT OF PROJECT PERSONNEL INTERNAL/EXTERNAL Female candidates from all Member States are particularly encouraged to apply. Vacancy Announcement No: VA2021_ISA_EXT_034 Duty Station: Austria Date of Issuance: 31 March 2021 Type of Appointment: Individual Service Agreement Employment Fraction: NonStaff-Regular Closing Date: 21 April 2021 Organizational Context The United Nations Industrial Development Organization (UNIDO) is the specialized agency of the United Nations that promotes industrial development for poverty reduction, inclusive globalization and environmental sustainability. The mission of the United Nations Industrial Development Organization (UNIDO), as described in the Lima Declaration adopted at the fifteenth session of the UNIDO General Conference in 2013, is to promote and accelerate inclusive and sustainable industrial development (ISID) in Member States. The relevance of ISID as an integrated approach to all three pillars of sustainable development is recognized by the 2030 Agenda for Sustainable Development and the related Sustainable Development Goals (SDGs), which will frame United Nations and country efforts towards sustainable development in the next decade. UNIDO’s mandate is fully recognized in SDG-9, which calls to “Build resilient infrastructure, promote inclusive and sustainable industrialization and foster innovation”. The relevance of ISID, however, applies in greater or lesser extent to all SDGs. Accordingly, the Organization’s programmatic focus is structured in four strategic priorities: Creating shared prosperity; Advancing economic competitiveness; Safeguarding the environment; and Strengthening knowledge and institutions.Each of these programmatic fields of activity contains a number of individual programmes, which are implemented in a holistic manner to achieve effective outcomes and impacts through UNIDO’s four enabling functions: (i) technical cooperation; (ii) analytical and research functions and policy advisory services; (iii) normative functions and standards and quality-related activities; and (iv) convening and partnerships for knowledge transfer, networking and industrial cooperation. Such core functions are carried out in Departments/Offices in its Headquarters, Regional Offices and Hubs and Country Offices. The Directorate of Digitalization, Technology and Agri-Business (DTA), headed by a Managing Director, coordinates and mainstreams the Fourth Industrial Revolution (4IR) in its technical cooperation, strategic, normative activities aiming at fostering the inclusive and sustainable development in the era of 4IR. The Directorate creates new and innovative technical cooperation deliverables in the areas of trade, investment, technology innovation and agro-industry and agri-business. The Directorate comprises the Department of Digitalization, Technology and Innovation (DTI) and the Department of Agri-Business (AGR).This position is located under the Department of Agri-Business (DTA/AGR). DTA/AGR provides a range of technical cooperation services to assist developing countries add value to the output of their agricultural sector and generate employment opportunities in off-farm activities for rural communities, thereby contributing to increased food security and a sustainable reduction of poverty. The department provides support for the development of agri-business corridors in developing countries in collaboration with International Financial Institutions. The Department drives the Organization’s mandates of creating shared prosperity and advancing economic competitiveness. It supports initiatives to build human capital and raise total factor productivity through focused vocational training and industrial skills development activities. With its programmes, the Department addresses the root causes of migration and helps alleviate migration pressures at the origin.The Sustainable Food Systems Division (DTA/AGR/SFS) promotes ISID through the promotion of food systems that deliver food and nutrition security without compromising economic, social, and environmental bases to generate food security and nutrition for future generations. The Division is responsible for identifying, developing and managing programmes to improve the competitiveness of the food and agribusiness sectors through access to support services, finance, markets and trade opportunities. The Division contributes to the capacity-building of food systems support institutions and skill development agencies through its advisory and convening activities. Project Context:190011: Agricultural in South Sudan presents an ideal foundation for economic growth, yet youth often do not have the knowledge or means to add value to agricultural goods, create enterprises around such work and scale-up businesses. In collaboration with UNDP, the project aims to empower youth in five targeted locations – Bor, Jubek, Rumbek, Torit and Yambio – through nurturing their entrepreneurial culture and market-linked skills and enhance their employability and productive engagement in economic activities. The project also seeks to increase the productivity and labour-absorptive capacities of agriculture and natural resource-linked value chains and private sector enterprises with a focus on young men and women. Over 8,000 urban and rural young people will benefit from vocational, entrepreneurship, market-linked and soft skills training, provision of small and micro enterprise start-up kits, job and employment creation through the development of inclusive value chains and private sector enterprises.DUTY STATION: Vienna, AustriaDURATION: 1 year (with possibility of extension) Main Functions Under the supervision of the Project Manager in the Sustainable Food Systems Divisions, the project specialist provides professional inputs to promote effective project implementation through appraising, adjusting and presenting project proposals, and monitoring programme implementation, identifying problems and utilizing information as an input to corrective actions to promote effective project management. Develops and administers technical cooperation projects, particularly: - Analysing economic, social and political factors which affect a sectoral or regional development programme in relation to relevant resolutions of the Organization's governing body and the Organization's policies and priorities; reflecting conclusions reached in sectoral or regional development plans, project proposals and formulations, and in the management coordination of ongoing development activities; - Analysing development needs and appraising the suitability of proposed programmes and projects in meeting these needs, recommending project approval to the Organization; - Identifying particular development project possibilities in relation to expressed governmental needs and the known capabilities and resources available to the Organization, assessing the relative feasibility and impact of proposed projects in country and regional plans; - Introducing into the project formulation process newly developed modalities, policies and practices, as well as alternative methods for independent evaluation of projects and proposals which are designed to improve the effectiveness and appropriateness of the Organization's project and programme planning and delivery processes; - Guiding, coordinating and integrating the drafting of project proposals and justifying them in terms of regional and sectoral development objectives; - Expediting and endorsing submission according to funding institution procedures of all required operational documents for approved projects; - Providing technical advice, guiding and orienting the efforts and contributions of consultants, project personnel, donors, institutions and governments towards the achievement of project objectives; - Assessing the degree of implementation of technical assistance project activities and resources; identifying problems and resource and financial deficiencies, and initiating and proposing corrective or alternative actions. Core Competencies WE LIVE AND ACT WITH INTEGRITY: work honestly, openly and impartially.WE SHOW PROFESSIONALISM: work hard and competently in a committed and responsible manner.WE RESPECT DIVERSITY: work together effectively, respectfully and inclusively, regardless of our differences in culture and perspective.WE FOCUS ON PEOPLE: cooperate to fully reach our potential –and this is true for our colleagues as well as our clients. Emotional intelligence and receptiveness are vital parts of our UNIDO identity.WE FOCUS ON RESULTS AND RESPONSIBILITIES: focus on planning, organizing and managing our work effectively and efficiently. We are responsible and accountable for achieving our results and meeting our performance standards. This accountability does not end with our colleagues and supervisors, but we also owe it to those we serve and who have trusted us to contribute to a better, safer and healthier world.WE COMMUNICATE AND EARN TRUST: communicate effectively with one another and build an environment of trust where we can all excel in our work.WE THINK OUTSIDE THE BOX AND INNOVATE: To stay relevant, we continuously improve, support innovation, share our knowledge and skills, and learn from one another. Education Advanced university degree in agriculture, agronomy, project management, busines administration, international relations, or another area relevant to agricultural value chain or agribusiness development. Languages Fluency in written and spoken English is required. Fluency and/or working knowledge of another official UN language, particularly French is desirable. Field of Expertise At least seven (7) years of professional experience in technical cooperation project management related to agricultural value chains or portfolio project management including some exposure at the international level is required. Exposure to the needs, conditions and problems in developing countries. Ability to research and analyze information, make linkages with the strategic vision of the Organization and recommend solutions. Ability to write in a clear and concise manner. Ability to work effectively in multi-cultural teams. This appointment is limited to the specified project(s) only and does not carry any expectation of renewal. Employees of UNIDO are expected at all times to uphold the highest standards of integrity, professionalism and respect for diversity, both at work and outside. Only persons who fully and unconditionally commit to these values should consider applying for jobs at UNIDO. All applications must be submitted online through the Online Recruitment System Correspondence will be undertaken only with candidates who are being considered at an advanced phase of the selection process.Selected candidate(s) may be required to disclose to the Director General the nature and scope of financial and other personal interests and assets in respect of themselves, their spouses and dependants, under the procedures established by the Director General. NOTE: The Director General retains the discretion to make an appointment to this post at a lower level. Project Specialist (Value Chain Development) Complete the personal history form and apply to this job now. Notice to applicants:UNIDO does not charge any application, processing, training, interviewing, testing or other fee in connection with the application or recruitment process.If you have received a solicitation for the payment of a fee, please disregards it. Vacant positions within UNIDO are advertised on the official UNIDO website.Should you have any questions concerning persons or companies claiming to be recruiting on behalf of UNIDO and requesting payment of a fee, please contact:recruitmentunido.org
Head of Pre-Clinical Development (m/w/d)
Iventa. The Human Management Group, Wien
Für ein spannendes Unternehmen suchen wir einen geeigneten Kandidaten zur Besetzung dieser Position. Review of monitoring visit reports Establish and track appropriate performance metrics in terms of monitoring Provide guidance and training to CRO/external CRAs Ensure quality of eTMF, conduct regular quality reviews Present at and provide support for investigator meetings/CRA trainings Medical-pharmaceutical, scientific or similar background, preferably academic Work experience in the pharmaceutical industry or CRO industry Previous work experience with Phase 2 or 3 studies A minimum of 5 years’ experience as a Clinical Research Associate Extensive co-monitoring experience Problem-solving abilities, excellent communication skills and manners Strong interpersonal skills Ability to work efficiently, independently and in a team environment Precise workstyle and deadline accuracy Willingness to travel up to 35% Excellent German language skills and fluent in English; both written and oral Good IT skills
Senior Research Associate (m/f/d)
Dr. Pendl & Dr. Piswanger GmbH, Wien
Research Associate Vienna, Full-Time, m/f/d At GoStudent, we work passionately every day to fulfill our mission in building the 1 global school Headquartered in Vienna and founded AOP Orphan is a European pioneer in the development, marketing and distribution of medicines for people with rare and complex diseases. To enhance our team in Vienna we are looking You will be responsible for: The quality of study data and for ensuring that studies are carried out according to study protocols, SOPs, ICH/GCP and regulations. You will be responsible for sponsor oversight in terms of monitoring (conducted Our client Spencer Stuart is one of the world’s leading global executive search and leadership consulting firms, specialized in chief executive, board director and senior executive roles. The growing and successful team in Vienna is hiring a talent with the right combination of skills and mindset – to join the research team in international recruitment. Senior Research Associate (m/f/d) You will be part of the industry consulting team, consisting of one senior consultant one Executive Assistant, and you. Your responsibilities: Take ownership in client engagements to understand client needs and advise clients around talent, organzitaional set up etc. Gather relevant information regarding the appropriate industries and target companies, including identifying potential candidates and sources. Represent clients effectively in the marketplace and present comprehensive output in terms of market feedback, evaluations, qualifierd candidates and assessment work. Take full responsibility for search and assessment projects, serving as a sparring partner towards both clients and partners of the firm. Your profile: Graduate degree from a competitive university; diverse educational backgrounds are welcome. 3 years work experience in a corporate function or another consulting firm where multiple projects and competing deadlines are the norm. Some domain expertise within a function or an industry that can be leveraged to advise clients. International experience (working or living) is an advantage as we are part of a global firm and engage internationally on a daily basis. Fluent in English and German (written & verbal); additional language skills are considered an advantage. Strong communicator and relationship builder with excellent analytical skills. Our offer: You will be part of a market leading organisation, their executives and board members across a variety of top leadership topics. Working with clients and colleagues from around the world in a truly international business environment. Delivering real impact through evidence-based research and methodologies. Spencer Stuart’s approach to leadership and asssessment is derived from 60years of experience. Professional and personal growth and a clear career path with multiple development and (international) progression opportunities. Broad exposure to the people and challenges faced by our industry-leading clients. The competitive salary package starts at EUR 60.000 p.a. plus bonuses and can be higher depending on your personal background and experience. If you are motivated by working globally with top business executives around leadership development and organizational cultures, then we are looking forward to your application to our Senior Consulant Susanna Pawlowsky ( s.pawlowskypendlpiswanger.at ), Code "A010567" Spencer Stuart can provide THE platform to harness your drive and curiosity
Research Associate
globe personal services, Wien
You will be responsible for: The quality of study data and for ensuring that studies are carried out according to study protocols, SOPs, ICH/GCP and regulations. You will be responsible for sponsor oversight in terms of monitoring (conducted AOP Orphan is a European pioneer in the development, marketing and distribution of medicines for people with rare and complex diseases. To enhance our team in Vienna we are looking Research Associate Vienna, Full-Time, m/f/d At GoStudent, we work passionately every day to fulfill our mission in building the 1 global school Headquartered in Vienna and founded Your role: You will shape decisions regarding what drugs, modes of actions and dosage regimens are best suited for achieving the desired therapeutic effect to help cancer patients. We seek for an open At BIOMIN we harness the power of science to support animal health and performance. By applying state-of-the-art and proprietary technology we deliver natural, sustainable and profitable Your responsibilities: Take ownership in client engagements to understand client needs and advise clients around talent, organzitaional set up etc. Gather relevant information regarding the appropriate industries and target QPS Austria GmbH is an international full-service contract research organization (CRO) in the area of preclinical and clinical research. To cover monitoring activities in predominantly At BIOMIN we harness the power of science to support animal health and performance. By applying state-of-the-art and proprietary technology we deliver natural, sustainable and profitable Senior Data Scientist Referenz-Nr.: JN -062021-2932133 Ort: Lenzing Anstellungsart: Permanent Firmenprofil Dealing with big data and generating value-adding insights out of them is
Sr Study Start Up Associate
ICON plc, Wien
At ICON, it's our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients' lives. Our 'Own It' culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development. That's our vision. We're driven by it. And we need talented people who share it. If you're as driven as we are, join us. You'll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you'll be helping shape an industry. As a Senior Study Start Up Associate at ICON, you'll work within a large-scale, fast-paced environment assisting the Study Start Up Team Lead in the development of the plan for country and site distribution and execution of SSU activities in assigned countries. We pride ourselves on our amazing company culture, where we work as one team to achieve industry-leading results. The role Responsible for performing feasibility, site identification, site contract negotiation, and other SSU activities. Provide country specific SSU expertise to Study Start Up team leads and project teams. Responsible for the preparation and coordination of submissions to regulatory, ethics, and other bodies. Develop, finalize, and review Master and Country Specific Subject Information Sheets/Informed Consent Forms. What you need A Bachelor's Degree or local equivalent and/or appropriate experience from the Medical/science background and/or discipline. A minimum of 3 years of experience or understanding of clinical study start up requirements and activities. Fluency in the local language and English is essential. Benefits of Working in ICON: Our success depends on the quality of our people. That's why we've made it a priority to build a culture that rewards high performance and nurtures talent. We offer very competitive salary packages. And to keep them competitive, we regularly benchmark them against our competitors. Our annual bonuses reflect delivery of performance goals - both ours and yours. We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans - and related benefits such as life assurance - so you can save and plan with confidence for the years ahead. But beyond the competitive salaries and comprehensive benefits, you'll benefit from an environment where you are encouraged to fulfil your sense of purpose and drive lasting change. ICON is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below. Click here to see other roles I'm currently recruiting for. ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology At ICON, it's our people that set us apart. 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Sr Study Start Up Associate
ICON plc, Wien
As a member of the Study Start Up Team, you will play an integral role in making sure that physicians at our research sites are prepared to start the trial of investigational, new pharmaceutical and biological products for clinical trials at their local practices. At ICON, it's our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients' lives. Our 'Own It' culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development. That's our vision. We're driven by it. And we need talented people who share it. If you're as driven as we are, join us. You'll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you'll be helping shape an industry. The Role Collect, prepare, review, approve, process and track regulatory and site level critical documents required for study site activation in accordance with ICON SOPs/WPs, Sponsor SOPs, applicable country regulations/guidelines and the principles of ICH/GCP. This may include: Prepare, review and approve Subject Information Sheets (SIS) and Informed Consent Forms (ICF) Prepare, review and negotiate Clinical Trial Agreements, budgets and any required ancillary agreements with assigned Study Sites, including the facilitation of the indemnification process, between Sponsor and Study Site. Collect, review, organize and assemble regulatory initial start-up and maintenance submission packages to Central EC/IRB, Local EC/IRB, Competent Authorities, any other local regulatory authorities as required by countries. Essential Country and Site document collection and review, ensuring that Sponsor and Investigator obligations are being met and are in compliance with applicable country requirements. Embrace and contribute to ICON's culture of delivery, quality and process improvement with a focus on internal stakeholders collaboration, enhancing processes, systems and tools, adding value to our business, shortening Site Activation timelines and meeting client's expectations. This will translate in predicting and delivering site activation within predicted timelines, and ahead of industry standards. What you need A bachelor's degree in Paralegal Studies, Juris Doctor (law) degree, or related experience is preferred SSU experience is required. Experience in a clinical research environment with specific experience in study contracts review and budget negotiation or in related field such as where contract or legal document review is a primary part of you role. Benefits of Working in ICON: Our success depends on the quality of our people. That's why we've made it a priority to build a culture that rewards high performance and nurtures talent. We offer very competitive salary packages. And to keep them competitive, we regularly benchmark them against our competitors. Our annual bonuses reflect delivery of performance goals - both ours and yours. We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans - and related benefits such as life assurance - so you can save and plan with confidence for the years ahead. But beyond the competitive salaries and comprehensive benefits, you'll benefit from an environment where you are encouraged to fulfil your sense of purpose and drive lasting change. ICON is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. 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Study Start Up Associate I
ICON plc, Wien
As a Study Start Up Associate I at ICON, you'll work as a member of the Study Start Up Team, you will play an integral role in making sure that physicians at our research sites are prepared to start the trial of investigational, new pharmaceutical and biological products for clinical trials at their local practices. The Role To review and negotiate clinical site investigator contracts and budgets. Stay connected with Investigative sites, sponsors and internal personnel regarding the status of contracts and contract-related documents Prepare and coordinate preparation of contractual documents and correspondence Facilitate the indemnification process between the study sponsor and the site. Perform regulatory document for maintenance e.g. amendments, periodic updates and safety letters. Prepare, review, submit and QC submissions to ethics, regulatory and other authorities to obtain clinical trial authorizations and approvals. Collect critical documents for IP release. What you need A bachelor's degree or related experience is preferred SSU experience is desirable but not required. German and English language skills Experience in a clinical research environment with specific experience in study submissions or contracts review and budget negotiation or in related field such as where submissions or contract or legal document review is a primary part of you role. Click here to see other roles I'm currently recruiting for. ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology At ICON, it's our people that set us apart. 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Lead Clinical Research Associate (m/f/d)
Octapharma Pharmazeutika Produktionsges.m.b.H., Wien
Lead Clinical Research Associate (m/f/d) Clinical Trial Leader (m/f/d) Austria (Vienna) Vienna JOB-ID 217333217333 JOB LEVEL: Experienced FUNKTIONSBEREICH: Clinical Operations ARBEITSZEIT: Full-time THE POSITION For our Therapeutic (Associate) Principal Scientist, Oncology Translational Science (m/f/d) Austria (Vienna) Vienna JOB-ID 214983 214983 JOB LEVEL: Experienced FUNKTIONSBEREICH: Research & Development Octapharma specializes in the development of highly pure pharmaceuticals made of human blood plasma. As part of a family-owned enterprise, Octapharma in Vienna is not only the largest production site, but also a successful research location of the Octapharma Group. Since our company continues to grow, we are now hiring for our team a Lead Clinical Research Associate (m/f/d) Location: Job Level: Professionals Department: Research and Development Working time: Full-time (38 hours/week) Your new challenges which will inspire you: Responsibility for sponsor´s monitoring oversight (incl. performance metrics, monitoring visit reports reviews, protocol deviations, training activities) Being the primary contact for CRO clinical monitoring team Conducting remote and on-site co-monitoring visits, interaction with clinical sites Involvement in site selections, qualification reviews Oversight of eTMF (incl. regular quality reviews) during the whole study including set-up Audit support, Inspection site preparation support Being an essential part of a sponsor project team operating globally, led by experienced project managers Your profile that will convince us: Biological or medical science background Minimum of 5 years’ experience in clinical research (as CRA or LCRA) in a CRO, pharmaceutical or biotechnology company Co-monitoring experience Strong organisational and interpersonal skills (presentation, documentation) Solution-oriented and positive approach, enjoying teamwork Professional use of the English language; both written and oral, German language knowledge beneficial Willingness to travel internationally up to 30% Wide range of tasks in an international setting, flexibility and personal responsibility Reliable employer with generous employee benefits and a salary customary in the market. Familiar setting of a family-owned enterprise with benefits such as Do & Co staff restaurant, extraordinary staff events and many more: Additional information: The minimum gross wage according to the collective agreement (chemical industry) for your new job is EUR 3.389,68. We strive to adapt your salary to your range of tasks and to your profile, which is why we are ready to pay wages higher than collectively agreed. T: 43 (1) 610 32 – 1301 About Octapharma As a family-owned company, Octapharma believes in investing to make a difference in people’s lives and has been doing so since 1983; because it’s in our blood. Our company values are Ownership, Integrity, Leadership, Sustainability and Entrepreneurship. In 2019, the Group achieved €2.2 billion in revenue, an operating income of €424 million and invested €232 million to ensure future prosperity. Octapharma employs more than 10,000 people worldwide, around 1,230 of them in Vienna, to support the treatment of patients in 118 countries with products across three therapeutic areas: Haematology (coagulation disorders), Immunotherapy (immune disorders) and Critical Care. Octapharma owns six state-of-the-art Production facilities in Austria, France, Germany (Dessau & Springe), Mexico and Sweden.
Study Start Up Associate II
ICON plc, Wien
ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life. Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well. As a Study Start Up Associate II "Medical Device" at ICON, you'll work as a member of the Study Start Up Team, you will play an integral role in making sure that physicians at our research sites are prepared to start the trial of investigational, new pharmaceutical and biological products for clinical trials at their local practices. The Role To review and negotiate clinical site investigator contracts and budgets. Stay connected with Investigative sites, sponsors and internal personnel regarding the status of contracts and contract-related documents Prepare and coordinate preparation of contractual documents and correspondence Facilitate the indemnification process between the study sponsor and the site. Perform regulatory document for maintenance e.g. amendments, periodic updates and safety letters. Prepare, review, submit and QC submissions to ethics, regulatory and other authorities to obtain clinical trial authorizations and approvals. Collect critical documents for IP release. What you need A bachelor's degree or related experience is preferred 2 year of SSU experience in Medical devices area. Local language (German) and English language skills Experience in a clinical research environment with specific experience in study submissions or contracts review and budget negotiation or in related field such as where submissions or contract or legal document review is a primary part of you role. Benefits of Working in ICON: Our success depends on the knowledge, capabilities and quality of our people. That's why we are committed to developing our employees in a continuous learning culture - one where we challenge you with engaging work and where every experience adds to your professional development. At ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future. ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below. Click here to see other roles I'm currently recruiting for. ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology ICON plc is a world-leading healthcare intelligence and clinical research organisation. 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Lead Clinical Research Associate (m/f/d) (39061)
octapharma Pharmazeutika Produktionsges.m.b.H., Wien
Career Opportunities: Lead Clinical Research Associate (m/f/d) (39061) Requisition ID 39061 - Posted 28/07/2021 - Austria - Vienna - Research and Development - Permanent position - Professionals Octapharma specializes in the development of highly pure pharmaceuticals made of human blood plasma. As part of a family-owned enterprise, Octapharma in Vienna is not only the largest production site, but also a successful research location of the Octapharma Group. Since our company continues to grow, we are now hiring for our team a Lead Clinical Research Associate (m/f/d) Location : Job Level: Department: Working hours: Professional Clinical R&D Full-time (38 hours/week) Your new challenges which will inspire you: Responsibility for sponsor´s monitoring oversight (incl. performance metrics, monitoring visit reports reviews, protocol deviations, training activities) Being the primary contact for CRO clinical monitoring team Conducting remote and on-site co-monitoring visits, interaction with clinical sites Involvement in site selections, qualification reviews Oversight of eTMF (incl. regular quality reviews) during the whole study including set-up Audit support, Inspection site preparation support Being an essential part of a sponsor project team operating globally, led by experienced project managers Your profile that will convince us: Biological or medical science background Minimum of 5 years’ experience in clinical research (as CRA or LCRA) in a CRO, pharmaceutical or biotechnology company Co-monitoring experience Strong organisational and interpersonal skills (presentation, documentation) Solution-oriented and positive approach, enjoying teamwork Professional use of the English language; both written and oral, German language knowledge beneficial Willingness to travel internationally up to 30% Wide range of tasks in an international setting, flexibility and personal responsibility Reliable employer with generous employee benefits and a salary customary in the market. Familiar setting of a family-owned enterprise with benefits such as Do & Co staff restaurant, extraordinary staff events and many more: Additional information: The minimum gross wage according to the collective agreement (chemical industry) for your new job is EUR 3.389,68. We strive to adapt your salary to your range of tasks and to your profile, which is why we are ready to pay wages higher than collectively agreed. We are looking forward to new, committed employees who join forces with us to promote our strong growth in order to keep enabling our patients to live a better life - because it is in our blood Is it in T: 43 (1) 610 32 – 1301 About Octapharma As a family-owned company, Octapharma believes in investing to make a difference in people’s lives and has been doing so since 1983; because it’s in our blood. Our company values are Ownership, Integrity, Leadership, Sustainability and Entrepreneurship.In 2019, the Group achieved €2.2 billion in revenue, an operating income of €424 million and invested €232 million to ensure future prosperity. Octapharma employs more than 10,000 people worldwide, around 1,230 of them in Vienna, to support the treatment of patients in 118 countries with products across three therapeutic areas: Haematology (coagulation disorders), Immunotherapy (immune disorders) and Critical Care. Octapharma owns six state-of-the-art Production facilities in Austria, France, Germany (Dessau & Springe), Mexico and Sweden.
Clinical Research Associate
Graduateland, Wien
Über AbbVie AbbVies Mission ist es innovative Medikamente zu entdecken, die im Heute schwerwiegende Gesundheitsprobleme lösen und die medizinischen Herausforderungen von morgen angehen. Wir streben danach, in verschiedensten therapeutischen Schlüsselbereichen einen bemerkenswerten Einfluss auf das Leben der Menschen auszuüben: Immunologie, Onkologie, Neurowissenschaften, Augenheilkunde, Virologie, Frauengesundheit und Gastroenterologie sowie Produkte und Dienstleistungen aus dem gesamten Portfolio von AbbVie im Bereich der Allergan-Aesthetics. Für weitere Informationen über AbbVie besuchen Sie uns bitte unter . Folgen Sie abbvie auf , , , und . Aufgaben: Aktivitäten im Rahmen der Studienvorbereitung: Country und Site Feasibility in Abstimmung mit der medizinischen Abteilung, Zentrenauswahl, Einholung aller relevanten Studienunterlagen sowie Einreichung bei EK/Behörde (Initial- wie auch Folgeeinreichungen; auch mittels VHP Verfahren), Unterstützung der Vertragsspezialistin bei Budget- und Vertragsverhandlungen, Training der Studienärzte und anderen Zentrums-Mitarbeitern vor der Zentrenaktivierung und während der Studie Monitoring: Überprüfung der ordnungsgemäßen Durchführung von klinischen Studien mittels On site- und Off site Visiten, Sicherstellung der Datenqualität durch SDR und SDV, Betreuung, Schulung und Motivation der Prüfzentren, um vereinbarte Ziel- und Zeitvorgaben (Rekrutierung, Dateneingabe etc.) einzuhalten, Vorbereitung und kontinuierliche Aktualisierung von studienbezogenen Dokumenten etc Administrative Tätigkeiten: Kontinuierliches Aktualisieren der Studienmanagementsysteme (wie CTMS, eTMF, etc.) mit dem Ziel jederzeit „audit/inspection ready“ zu sein, Dokumentation von Visiten und Protokollabweichungen im CTMS im Studienverlauf, Koordination der Bezahlung anhand der Studienvereinbarungen Qualifikationen Naturwissenschaftliches Studium oder eine vergleichbare Ausbildung im Gesundheitswesen Idealerweise 2 Jahre Berufserfahrung als Clinical Monitor oder CRA Exzellentes Organisationstalent, analytisches Denkvermögen, ausgezeichnete soziale Kompetenz und Überzeugungskraft Hohes Maß an Flexibilität, Teamfähigkeit, Kommunikationsstärke und Durchsetzungsvermögen Freude an Reisetätigkeit an bis zu 5 Tagen/Monat Sehr gute Englischkenntnisse, weitere Fremdsprachenkenntnisse von Vorteil Sicherer Umgang mit MS Office Wir bieten Ihnen eine herausfordernde, spannende Tätigkeit mit einem interessanten Benefitpaket. Diese Tätigkeit ist mit einem Bruttomonatsbezug von EUR 3.200, dotiert. In Abhängigkeit von Ihrer persönlichen Qualifikation und Erfahrung ist die Bereitschaft zur Überbezahlung gegeben. Werden Sie Teil unseres dynamischen und internationalen Teams, das Top-Talente verschiedener Hintergründe vereint. Wir freuen uns auf Ihre Bewerbung Reisebereitschaft Ja, 25 % der Zeit Stellentyp Erfahren Zeitplan Vollzeit Job Level Code IC Equal Employment Opportunity At AbbVie, we value bringing together individuals from diverse backgrounds to develop new and innovative solutions for patients. As an equal opportunity employer we do not discriminate on the basis of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information gender identity or expression, sexual orientation, marital status, protected veteran status, or any other legally protected characteristic. Apply now Remember to mention that you found this position on Graduateland
Clinical Research Associate (m/w/d)
Iventa. The Human Management Group, Wien
AbbVies Mission ist es, innovative Medikamente zu entdecken und wir streben danach, in verschiedensten therapeutischen Schlüsselbereichen einenbemerkenswerten Einfluss auf das Leben der Menschen auszuüben: Immunologie, Onkologie, Neurologie, Augenheilkunde, Virologie und Gastroenterologie sowiemit Produkten und Dienstleistungen aus dem Bereich der Allergan-Aesthetics.Du denkst gerne auch einmal quer und schaust über den Tellerrand hinaus? Du willst einen Beitrag für die Lebensqualität von Millionen von Patienten weltweitleisten? Dann lerne uns kennen und werde Teil eines Teams, das einen Unterschied macht.Wir bauen unser Team aus und suchen für unseren Standort in Wien. Studienvorbereitung: Country und Site Feasibility in Abstimmung mit der medizinischen Abteilung, Zentrenauswahl, Einholung aller relevanten Studienunterlagen sowie Einreichung bei EK/Behörde, Unterstützung der Vertragsspezialistin bei Budget- und Vertragsverhandlungen, Training der Studienärzte und Zentrums-Mitarbeitern vor der Zentrenaktivierung und während der Studie Monitoring: On site- und Off site Visiten zur Überprüfung der ordnungsgemäßen Durchführung von klinischen Studien, Sicherstellung der Datenqualität durch SDR und SDV, Betreuung, Schulung und Motivation der Prüfzentren zur Ziel- und Zeitvorgabeneinhaltung, Vorbereitung und Aktualisierung von studienbezogenen Dokumenten, etc. Administrative Tätigkeiten: Aktualisierung der Studienmanagementsysteme (wie CTMS, eTMF, etc.) mit dem Ziel jederzeit „audit/inspection ready” zu sein, Dokumentation von Visiten und Protokollabweichungen im CTMS im Studienverlauf, Koordination der Bezahlung anhand der Studienvereinbarungen Idealerweise mindestens 1 Jahr Berufserfahrung als Clinical Monitor, CRA oder Studienkoordinator Exzellentes Organisationstalent, analytisches Denkvermögen, ausgezeichnete soziale Kompetenz und Überzeugungskraft Hohes Maß an Flexibilität, Teamfähigkeit, Kommunikationsstärke und Durchsetzungsvermögen Freude an Reisetätigkeit an bis zu 5 Tagen/Monat , Teilnahme in internationalen Meetings Sehr gute Englischkenntnisse, weitere Fremdsprachenkenntnisse von Vorteil Sicherer Umgang mit MS Office Arbeiten bei AbbVie sollte für Dich nicht nur ein Job, sondern eine Leidenschaft sein. Wir suchen nach Menschen, die wirklich etwas bewegen und mit uns gemeinsam Patienten in den Mittelpunkt stellen wollen. Eine offene Unternehmenskultur steht bei uns an erster Stelle und das spürt man – bei uns hast Du die Möglichkeit, von Anfang an mit anzupacken, Dich einzubringen und wirklich etwas zu bewegen. Wir bieten Dir eine herausfordernde, spannende Tätigkeit mit einem interessanten Benefitpaket. Diese Tätigkeiten sind mit einem Jahresbruttogehalt ab EUR 44.800 dotiert. In Abhängigkeit von Deiner persönlichen Qualifikation und Erfahrung ist die Bereitschaft zur Überzahlung gegeben. AbbVie zeichnet sich durch Diversität und Internationalität aus. Daher begrüßen wir Vielfalt bei unseren Bewerbern, insbesondere auch von chronisch kranken und behinderten Menschen. Machen wir gemeinsam den Unterschied! Erfahre mehr über AbbVie Österreich auf www.abbvie.at.
Clinical Research Associate (m/w/d)
Iventa. The Human Management Group, Wien
AbbVies Mission ist es, innovative Medikamente zu entdecken und wir streben danach, in verschiedensten therapeutischen Schlüsselbereichen einen bemerkenswerten Einfluss auf das Leben der Menschen auszuüben: Immunologie, Onkologie, Neurologie, Augenheilkunde, Virologie und Gastroenterologie sowie mit Produkten und Dienstleistungen aus dem Bereich der Allergan-Aesthetics. Du denkst gerne auch einmal quer und schaust über den Tellerrand hinaus? Du willst einen Beitrag für die Lebensqualität von Millionen von Patienten weltweit leisten? Dann lerne uns kennen und werde Teil eines Teams, das einen Unterschied macht. Wir bauen unser Team aus und suchen für unseren Standort in Wien. Studienvorbereitung: Country und Site Feasibility in Abstimmung mit der medizinischen Abteilung, Zentrenauswahl, Einholung aller relevanten Studienunterlagen sowie Einreichung bei EK/Behörde, Unterstützung der Vertragsspezialistin bei Budget- und Vertragsverhandlungen, Training der Studienärzte und Zentrums-Mitarbeitern vor der Zentrenaktivierung und während der Studie Monitoring: On site- und Off site Visiten zur Überprüfung der ordnungsgemäßen Durchführung von klinischen Studien, Sicherstellung der Datenqualität durch SDR und SDV, Betreuung, Schulung und Motivation der Prüfzentren zur Ziel- und Zeitvorgabeneinhaltung, Vorbereitung und Aktualisierung von studienbezogenen Dokumenten, etc. Administrative Tätigkeiten: Aktualisierung der Studienmanagementsysteme (wie CTMS, eTMF, etc.) mit dem Ziel jederzeit „audit/inspection ready” zu sein, Dokumentation von Visiten und Protokollabweichungen im CTMS im Studienverlauf, Koordination der Bezahlung anhand der Studienvereinbarungen Idealerweise mindestens 1 Jahr Berufserfahrung als Clinical Monitor, CRA oder Studienkoordinator Exzellentes Organisationstalent, analytisches Denkvermögen, ausgezeichnete soziale Kompetenz und Überzeugungskraft Hohes Maß an Flexibilität, Teamfähigkeit, Kommunikationsstärke und Durchsetzungsvermögen Freude an Reisetätigkeit an bis zu 5 Tagen/Monat , Teilnahme in internationalen Meetings Sehr gute Englischkenntnisse, weitere Fremdsprachenkenntnisse von Vorteil Sicherer Umgang mit MS Office Arbeiten bei AbbVie sollte für Dich nicht nur ein Job, sondern eine Leidenschaft sein. Wir suchen nach Menschen, die wirklich etwas bewegen und mit uns gemeinsam Patienten in den Mittelpunkt stellen wollen. Eine offene Unternehmenskultur steht bei uns an erster Stelle und das spürt man – bei uns hast Du die Möglichkeit, von Anfang an mit anzupacken, Dich einzubringen und wirklich etwas zu bewegen. Wir bieten Dir eine herausfordernde, spannende Tätigkeit mit einem interessanten Benefitpaket. Diese Tätigkeiten sind mit einem Jahresbruttogehalt ab EUR 44.800 dotiert. In Abhängigkeit von Deiner persönlichen Qualifikation und Erfahrung ist die Bereitschaft zur Überzahlung gegeben. AbbVie zeichnet sich durch Diversität und Internationalität aus. Daher begrüßen wir Vielfalt bei unseren Bewerbern, insbesondere auch von chronisch kranken und behinderten Menschen. Machen wir gemeinsam den Unterschied Erfahre mehr über AbbVie Österreich auf www.abbvie.at.
Postdoctoral Research Associate (40 h/week)
Universität für Bodenkultur Wien, Wien
University of Natural Resources and Life Sciences Vienna – responsibility for Humans and Nature. We work for the sustainable use and protection of natural resources. The Department of Forest- and Soil Sciences, Institute of Forest Entomology, Forest Pathology and Forest Protection is currently seeking a Postdoctoral Research Associate (Reference code: 172) Extent of employment: 40 hours per week Duration of employment: October 2021, limited to 6 years Gross monthly salary and pay grade in terms of collective agreement for university staff (payable 14 times per year): B1 lit. b, € 3.945,90 The successful applicant works predominantly in the working group forest pathology of the institute. The research focus depends on current projects at the institute, collaborative opportunities between staff members as well as the expertise and interests of the appointed candidate. Completion of postdoctoral lecturer qualification (“Habilitation”) within the employment period will be encouraged. Responsibilities Independent research and publishing in the fields of forest pathology and/or forest mycology Teaching in forest pathology, forest protection, mycology and/or ecology in Bachelor and Master programs at BOKU Co-supervision of Bachelor, Master and Doctoral theses Acquisition, execution and management of third-party funded projects Administrative tasks at the institute Engagement in the academic self-administration and in committees of the Department of Forest and Soil Sciences and/or the University of Natural Resources and Life Sciences, Vienna Required skills and qualifications Diploma/Master degree in Biology, Forest, Agricultural or Plant Sciences, Plant Health and Plant Protection or other equivalent university degree Excellent expertise and research experience in the fields of Forest/Plant Pathology, Mycology, Plant Sciences, and/or Molecular Ecology (applied in the aforementioned fields of research) Desirable skills and qualifications Scientific publications in the above-mentioned fields (preferentially connected to forests) Record of third-party funded projects Experience in academic teaching and supervision of student theses Know-how, methodological competence and laboratory experience in molecular ecology Experience in conducting laboratory and field studies Profound knowledge in statistics, expertise in data analysis and experience with appropriate software programs Knowledge in related disciplines (e.g. forest/plant protection, forest entomology, silviculture, ecology) Experience in knowledge transfer (oral and written) to various target audiences Excellent language skills in German and English (oral and written); German can also be learnt after starting the job National and international scientific mobility National and international collaborations High capability to conduct scientific work independently, goal-oriented and timely Excellent communication and cooperation skills to work in a team Driving licence Applications can be submitted until: 3rd of October 2021 University of Natural Resources and Life Sciences Vienna seeks to increase the number of its female faculty and staff members. Therefore qualified women are strongly encouraged to apply. In case of equal qualification, female candidates will be given preference unless reasons specific to an individual male candidate tilt the balance in his favour. People with disabilities and appropriate qualifications are specifically encouraged to apply. Please send your job application incl. CV List of publications (in SCI-listed / non SCI-listed journals), congress contributions, third-party projects, teaching and supervision activities Short draft concept of planned research activities as part of the position (max. 3 A4-pages) to Personnel department, University of Natural Resources and Life Sciences, Peter-Jordan-Straße 70, 1190 Vienna; E-Mail: kerstin.buchmuellerboku.ac.at. (Reference code: 172) For more information about this position, please conact: Univ.Prof. Dr. Thomas Kirisits (43-1-47654-91611, E-Mail: thomas.kirisitsboku.ac.at) More information about BOKU, the Department of Forest- and Soil Sciences and the Institute of Forest Entomology, Forest Pathology and Forest Protection can be found on the following websites: www.wabo.oku.ac.at and www.wabo.boku.ac.at/ifff. We regret that we cannot reimburse applicants travel and lodging expenses incurred as part of the selection and hiring process.
CRA or Senior CRA (m/w/d) - Medical Devices
IQVIA Argentina, Wien
EMBRACE YOUR PASSION TO DRIVE HEALTHCARE FORWARD Take your therapeutic expertise to the next level and help drive the evolution of clinical development for a variety of sponsors. As a Clinical Research Associate within our full-service model, you’ll have the opportunity to embrace your passion for a specific therapeutic area and work with cutting-edge technology developed specifically for CRAs by CRAs. With access to world-class training and professional development, we’ll give you the tools you need to create the career you want. Full Time Level: Entry-level, Mid-level, Senior-level What makes CRAs aligned to our full-service model successful? Check out the top traits we're looking for and see if you have the right mix.
Postdoctoral Research Associate (40 h/week)
Universität für Bodenkultur Wien, Wien
Postdoctoral Research Associate (40 h/week) University of Natural Resources and Life Sciences Vienna - responsibility for Humans . We work for the sustainable use and protection of natural resources. The Department of Crop Sciences, Institute of Vegetables and Ornamentals is currently seeking a Postdoctoral Research Associate (Reference code: 76) Extent of employment: 40 Hours per Week Duration of employment: limited for 6 years (with the option of permanent employment) Gross monthly salary and pay grade in terms of collective agreement for university staff (payable 14 . b, € 3.945,90 Responsibilities Independent teaching in German and English as well as research in the field of horticulture on a national and international level with a focus on the value chain of herbs, spices, medicinal plants in times of climate change Analyses of growth media and plants Plant physiology and quality-building measures Development of an independent research profile (with the aim of habilitation desired) Supervision of students (bachelor, master and dissertation theses) Submission and implementation of national and international research projects and administration of competitively acquired third-party funds Organizational activities in the field of teaching and research as well as academic selfadministration at the Institute of Vegetables and Ornamentals Participation in the design and implementation of the experiments in the field and laboratory as well as in the Research Stations Collaboration in the interdisciplinary fields of competence Participation in university self-administration, especially participation in the development of the Institute of Vegetables and Ornamentals and of the Department of Crop Sciences Regular publication of research results in SCI journals and transfer of knowledge Maintenance of the institute’s websites Required skills and qualifications Doctoral degree/PhD Diploma degree in Horticulture, Agronomy, Biology, Biochemistry or a comparable subject Scientific work experience (projects) Publication activity in peer-reviewed journals Very good experience in laboratory analyses Experience in one of the following areas: o Quality-building measures in cultivation and post-harvest o Spectrometry and HPLC . C1 level) and English Driving licence B Postdoc experience in the relevant field Further knowledge in planning of experiments and statistics Willingness to work regularly in the field, in the greenhouse and in the laboratory as well as in experimentation Desirable skills and qualifications Organisational skills Ability to integrate into a team and to lead a working group Good integration into the scientific community Good experience in project and third-party funding acquisition and management International experience, especially in the field of horticulture Presentation experience of scientific results in front of the national and international audience Teaching experience in the relevant area Programming and modeling knowledge and experience Basic knowledge of another European language, spoken and written Applications can be submitted until: 4th of May 2021 University of Natural Resources and Life Sciences Vienna seeks to increase the number of its female . Therefore qualified women are strongly encouraged to apply. In case of equal qualification, female candidates will be given preference unless reasons specific to an individual male . People with disabilities and appropriate qualifications are specifically encouraged to apply. Please send your job application incl. motivation letter CV List of publications and projects with the role in them .D. & Master thesis, PostDoc activity, language skills, etc. Driving licence Letters of recommendation to Personnel department, University of Natural Resources and Life Sciences, Peter-Jordan-Straße 70, 1190 Vienna; E-Mail: kerstin.buchmuellerboku.ac.at. (Reference code: 76) We regret that we cannot reimburse applicants travel and lodging expenses incurred as part of the . www.boku.ac.at In your application, please refer to myScience.at and reference JobID 29216 .
Bioinformatics Scientist - Junior/Senior (m/f/d)
Platomics GmbH, Wien
Bioinformatics Scientist - Junior/Senior (m/f/d) (Associate) Principal Scientist Bioinformatics Software Engineer (m/f/d) Austria (Vienna) Vienna JOB-ID 219593219593 JOB LEVEL: Experienced FUNKTIONSBEREICH: Research & Development Data Steward Computational Biology (m/f/d) Austria (Vienna) Vienna JOB-ID 219496219496 JOB LEVEL: Experienced FUNKTIONSBEREICH: Research & Development ARBEITSZEIT: Full-time THE POSITION Platomics develops a global marketplace for personalized medicine to make the future of molecular diagnostics available today. We are a young vibrant team and apply the most advanced computing technologies to enable big data processing and analysis in healthcare. Our backgrounds are in bioinformatics, genetics, software development, and mathematics. As a Junior Bioinformatics Engineer you will work at the core of the Platomics team where you have the opportunity to directly influence the way how personalized medicine is going to impact the future. Bioinformatics Scientist (full-time) Junior/Senior (m/f/d) We are looking for Junior and Senior Bioinformatics Scientists As a Bioinformatics Scientist you have the following responsibilities: Develop new approaches and algorithms for the clinical interpretation of NGS data Critically analyze large NGS datasets using in-house tools and build custom tools when needed Contribute to the codebase with stable and tested production grade code Develop reproducible analysis code for research and development purposes Collaborate closely with bioinformaticians, molecular biologists, and software engineers Communicate analysis results and conclusions to internal stakeholders Required Qualifications: University degree in bioinformatics, molecular biology or a related discipline, or 4 years of experience working in a bioinformatics role Strong experience in analyzing NGS data (including RNA-seq and DNA-seq) Solid understanding of Human Genetics Comfortable with writing clean and reusable Python code for bioinformatics applications Enthusiasm and flexibility to work in interdisciplinary teams Not afraid of complex problems Preferred Qualifications: Familiarity with Sequence Variant analysis and Variant Classification frameworks (e.g. ACMG-AMP) PhD in bioinformatics or molecular biology Knowledge of the algorithmic workings of modern variant calling packages (preferably GATK) Experience with CNV calling and structural variant analysis Strong publication record and demonstrated scientific problem solving skills Experience with Docker or other containerization systems Familiarity with Workflow managers (nextflow, argo, airflow) Experience in working with clinical NGS data We offer: An interdisciplinary and dedicated team Exciting challenges in a fast-evolving domain Opportunity to work on cutting-edge technologies The Platomics office is very conveniently located close to Praterstern, easily reachable via U1, U2, S-Bahn and ÖBB. We offer flexible working arrangements. You will earn a salary of minimum €35.784 per year as a career entry level (according to IT-KV). Willingness for over-payment is given for candidates with proper experience and/or qualifications. If you are interested in strengthening our development team please e-mail your CV, optionally including your GitHub/Kaggle/Datacamp profiles.