Clinical Research Associate - Jobs

Study start up CRA, Austria ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. As a CRA II at ICON, you will design and analyse clinical trials,

activities as assigned Your expertise and ideal skill set Medical-pharmaceutical or scientific university degree At least 5 years experience in clinical research Previous experience as a Clinical Trials Associate/Assisstant, Clinical Research Associate or similar Knowledge of the pharmaceutical industry or CRO industry and of the global clinical trials...

Join IQVIA as a Clinical Research Associate I or II (m/w/d) home-based throughout Austria in our single sponsor department, and advance your career in clinical research. You’ll enjoy the stability and resources of a leading, global contract research organization while...

Join IQVIA as a Clinical Research Associate II or Senior Clinical Research Associate I (m/w/d) home-based throughout Austria in our single sponsor department, and advance your career in clinical research. You’ll enjoy the stability and resources of a leading, global contract research organization while...

Description Agilent is a global leader in laboratory and clinical technologies; we are passionate about bringing great science to life. Our commitment to quality and innovation supports cutting-edge life science research, patient diagnostics, and ensures the safety of water, food, and pharmaceuticals. As scientists and clinicians pursue...

You are an excellent organizer and have outstanding social skills and persuasive ability? Then this key role as a Clinical Research Associate is exactly right for you! As a research-based biopharmaceutical company, AbbVie is one of the most successful companies in the industry internationally and a top...

AbbVie in Vienna is looking for a Clinical Research Associate to join their dynamic Clinical Research Team. In this role, you ll manage site activities for global clinical trials and ensure compliance with internal and external guidelines. Ideal candidates should possess a degree in health sciences and experience in clinical research.

proofread Clinical Evaluation Reports and associated documents to assess the safety and performance of a range of MED-EL products, in accordance with applicable regulations Build up the necessary knowledge regarding MED-EL products Collaboration with other departments within MED EL, and with external partners Profile

Tenure Track Professor of Experimental Cellular Immunotherapy Identification number: KA-HAEMA-2026-003788 We are looking for an excellent researcher with great potential to develop an internationally recognized research agenda in the field of experimental cellular immunotherapy. The Clinical Division of Rheumatology and Immunology and the Clinical Division

For candidates based in Austria, we offer a market-competitive gross annual salary starting at €58,500, depending on your qualifications and relevant professional experience. Please apply with your English CV. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life...

Your main tasks and responsibilities Medical revision and compilation of outgoing text documents (e.g. PIL, PI, SPC, DSURs/PSURs) Answering of medical enquiries associated with the use of any of the company’s products Maintenance of a database for medical enquiries Supervision and maintenance of the in-house literature database Managing the publications process related to clinical studies conducted by

IQVIA currently offers the exciting opportunity for a (Sr.) Site Activation Specialist (m/w/d) to work in the Country Site Activation Department in our Vienna office Austria. In this role you will perform tasks at a country level associated with clinical research site activation activities in accordance with applicable...

Support evidence generation through externally sponsored research, real-world evidence initiatives, registries, and observational studies, ensuring compliance with applicable SOPs, GCP, and audit requirements. Oversee scientific engagement processes including timely and balanced handling of medical enquiries and appropriate escalation where needed.