Clinical Affairs Specialist, Sports Medicine Devices

About the Job Join Excelya, whereAudacity, Care, and Energydefine who we are and how we work. We believe in creating bold solutions and fostering an inclusive environment where collaboration and individual growth go hand in hand. We are currently looking for a Medical Writer focused on Clinical Evaluation for Medical Devices to join our growing team. This...

**About the Job** Join Excelya, where **Audacity, Care, and Energy** define who we are and how we work. We believe in creating bold solutions and fostering an inclusive environment where collaboration and individual growth go hand in hand. We are currently looking for a Medical Writer focused on Clinical Evaluation for Medical Devices to join our growing...

About the Job Join Excelya, where Audacity, Care, and Energy define who we are and how we work. We believe in creating bold solutions and fostering an inclusive environment where collaboration and individual growth go hand in hand. We are currently looking for a Medical Writer focused on Clinical Evaluation for Medical Devices to join our growing team. This...

Regulatory Affairs Officer - Lyon, France (F/M)Join to apply for the Regulatory Affairs Officer - Lyon, France (F/M) role at Astek.About UsAlsinova, a subsidiary of the Astek Group, specializes in Life Sciences. We support pharmaceutical, biotech, and medtech companies with expertise in regulatory affairs, clinical development, data, quality, and...

A leading health company in Lyon seeks a Medical Writer focused on Clinical Evaluation for Medical Devices. You will develop and maintain clinical evaluation documentation, perform scientific literature searches, and write Clinical Evaluation Plans and Reports. The ideal candidate has at least 2 years of experience in writing Clinical Evaluation Reports and...

A leading medical device company in Lyon is looking for a passionate Regulatory Affairs Manager to lead regulatory and compliance projects across various business units. Key responsibilities include managing a team, developing regulatory strategies, and ensuring compliance with ISO standards. The ideal candidate has a Master’s degree and extensive...

A leading health company in Lyon is looking for an experienced Medical Writer focused on Clinical Evaluation for Medical Devices. This role involves developing clinical evaluation documentation, conducting literature searches, and supporting regulatory submissions. Ideal candidates should have a degree in life sciences, 2 years of related experience, and...

A leading mid-size CRO in Lyon is seeking a motivated Medical Writer focused on Clinical Evaluation for Medical Devices. You will work on projects that advance medical technologies while contributing to CE marking submissions and reports. Ideal candidates will have a degree in life sciences, at least 2 years of experience in clinical writing, and be...

What We Will Accomplish TogetherAlsinova, asubsidiary of the Astek Group, is a consulting firm specialized inLife Sciences. We support pharmaceutical, biotech, and medtech companies by providing high-level expertise inregulatory affairs, clinical development, data, quality, and pharmacovigilance. To support one of our major partners in thein vitro...

**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...