Lyon Medpace
experience, CRO experience preferred; 5+ years of Project Manager/Clinical Trial Manager experience at a CRO... Manage site quality, including direct supervision of project Clinical Research Associates and monitoring deliverables...
Paris Chipiron
sciences (minimum Master's degree). At least 3 years of experience in Clinical Affairs within the medical device industry... and analyze clinical data in collaboration with medical and statistical teams. Who We Are Chipiron is revolutionizing the...
Le Pont-de-Claix, Isère BD
management, negotiation, and communication skills. Extensive knowledge of U.S. medical device regulations, Good Clinical... for regulatory questions. About You: Experience in regulatory affairs and R&D within the pharmaceutical and medical device...
Lyon Medpace
-to-have Strong understanding of medical imaging technologies and workflows in clinical trials. Knowledge of regulatory standards and quality... biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe...
Lyon Medpace
-to-have Strong understanding of medical imaging technologies and workflows in clinical trials. Knowledge of regulatory standards and quality... biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe...
Le Pont-de-Claix, Isère BD
Affairs Team Member. In this role, you will be responsible for representing medical affairs in project teams to ensure the... in a scientific field, such as a master’s degree, PhD, PharmD, or MD. You must be familiar with Medical Device standards, such as ISO...