Clinical Trial Manager

Job Summary: Medpace is the leading CRO for Biotech companies and is continuing to add Clinical Trial Managers of different experience levels to join our Clinical Trial Management Group in Lyon. Clinical Trial Managers with expertise in Oncology/Cardiovascular/Endocrine/Metabolic are welcome to continue to work in their area of expertise or to expand to a...

Job Summary: Our global activities are growing rapidly, and we are currently seeking a full-time, office-based Clinical Trial Assistant to join our Clinical Trial Management team in Lyon. This position will work in a team to accomplish tasks and projects that are instrumental to the company’s success. If you want an exciting career where you use your...

Job Summary: Our global activities are growing rapidly, and we are currently seeking a full-time, office-based Clinical Trial Assistant to join our Clinical Trial Management team in Lyon. This position will work in a team to accomplish tasks and projects that are instrumental to the company’s success and is suited for an Entry-level or recent graduate...

Job Summary: Medpace is the leading CRO for Biotech companies and is continuing to add Clinical Trial Managers of different experience levels to join our Clinical Trial Management Group in France, particularly in our Lyon office. Clinical Trial Managers with expertise in Neuroscience and CNS are welcome to continue to work in their area of expertise or to...

**Job Opening** MaaT Pharma is a clinical-stage biotechnology company and industry leader in microbiome therapies in oncology, leveraging our whole ecosystem restoration approach to develop biotherapies to treat serious diseases. We are driven by our pioneering spirit, and we are the first microbiome-derived drug development company listed in continental...

**Responsibilities **- Communicate and collaborate on global study activities; working closely with the project coordinator and clinical trial manager - Ensure timely delivery of recurrent tasks consistently with a high degree of accuracy - Compile and maintain project-specific status reports within the clinical trial management system - Interact with the...

Job Summary: Responsibilities: - Communicate and collaborate on global study activities; working closely with the project coordinator and clinical trial manager - Ensure timely delivery of recurrent tasks consistently with a high degree of accuracy - Compile and maintain project-specific status reports within the clinical trial management system - Interact...

Job Summary: Responsibilities: - Communicate and collaborate on global study activities; working closely with the project coordinator and clinical trial manager - Ensure timely delivery of recurrent tasks consistently with a high degree of accuracy - Compile and maintain project-specific status reports within the clinical trial management system - Interact...

**Job summary**: As a **Clinical Research Associate **you will be expected to actively participate in and manage the recruitment of potential investigators and perform CA and EC submissions. You will be responsible for monitoring of clinical sites, maintenance of study files, conduct of pre-study and initiation visits, liaison with vendors and other duties....

**Job summary**: As an experienced **Clinical Operations Manager **you will be expected to develop and grow the team in France and support clients relationships for the assigned region. Reporting to the Executive Director Clinical Operations, you will be a key member of the **Clinical Operations team.** We are searching for an experienced, ambitious and...

**Presentation of the company**: AUROBAC THERAPEUTICS is a biopharmaceutical company created in 2022 by 3 renowned life sciences innovation companies, Boehringer Ingelheim, Evotec and bioMérieux, to become a global leader in the fight against bacterial infections, Antimicrobial Resistance (AMR) and their consequences in acute hospital settings such as...

Vous êtes passionné(e)s par le monde des sciences de la vie et de la recherche clinique ? Vous souhaitez évoluer dans un environnement international dynamique et collaboratif où votre expertise a un impact direct sur la vie des millions de personnes ? Rejoignez Aixial Group et contribuez à façonner l’avenir de la recherche clinique ! **Qui...

Job Summary: Due to continuous business growth and a strong study pipeline, we are currently looking to hire Project Coordinators to join our successful and growing France team and engage in clinical trial management on a day-to-day level. This position will work with our operational teams to accomplish tasks and projects that are instrumental to the...

Due to continuous business growth and a strong study pipeline, we are currently looking to hire Project Coordinators to join our successful and growing France team and engage in clinical trial management on a day-to-day level. This position will work with our operational teams to accomplish tasks and projects that are instrumental to the company’s success....

Freelance Clinical Research Associate at ClinChoice (View all jobs) France ClinChoice is a global full-service CRO dedicated to professional development and providing an excellent work-life balance, with a quality-focused, collaborative “one-team” culture. We are looking for a dynamic person to join our in-house team as a Freelance Clinical Research...

Job Summary: Our clinical operations activities are growing rapidly, and Medpace currently has multiple full-time leadership openings within our Clinical Operations team. This is a position with tremendous visibility within the company that plays a critical role in the financial, operational, and customer service success of our clinical trials....

Job Summary: Our clinical operations activities are growing rapidly, and we are currently seeking a full-time, office-based in Lyon, Regulatory Submissions Manager to join our Clinical Operations team. This position plays a key role in the clinical trial management process at Medpace. If you want an exciting career where you use your previous expertise and...

**Job summary**: As a **Regulatory Specialist **you will be expected to actively participate in all start up activities and perform CA and EC submissions. You will be responsible for communication with Regulatory Authorities and Ethics Committees and function as an expert for Regulatory issues in France. Reporting to **Clinical Operations Manager**, you will...

Accelerate your career in medical writing with a dynamic and multicultural team at Alerys, a global vaccine leader. As a Senior Medical Writer, you will play a key role in writing, coordinating, and managing clinical and regulatory documents for our laboratories.About the RoleWe are seeking a highly experienced Medical Writer to join our team. Your main...

Job Summary: Our imaging services are growing rapidly, and we are currently seeking a full-time, office-based **Project Coordinator** to join our team. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you. Responsibilities: - Review incoming medical...