🔎 Title: Clinical Project Manager

📍 Location: Greater Lyon, France (remote work possible)

✉️ Contact: [email protected]

🔸 The company

Are you looking for your next challenge?

Are you looking for the next step in your Clinical career ?

If yes, join a well established, growing company designing, developing and producing orthopedic devices that change the lives of patients.

To further support the growth of their clinical department this company has released an exciting position for a Clinical Project Manager to work alongside their Directeur Clinical Affairs.

This is a great opportunity to join a close knit team with one vision, surrounded by other senior experts in their field.

You can be sure that no two days will be the same! You’ll enjoy a wide variety of responsibilities covering various elements and work on international market.

🔹 The Opportunity

You will have the opportunity to join the team and shape your role as a Medical Writer where you will have autonomy and... directly impact the products from a clinical perspective. As well as writing CERs, writing clinical protocols and handling data, you will also have the opportunity to expand your knowledge into other clinical activities such as study management and study design. With the Medical Device Regulation in full force, you will ensure that all reports and data (existing & new) are kept compliant with the relevant regulations and highlight important information in cross-functional meetings. This is also an opportunity to experience new and exciting markets as the company continues to expand globally.

🔸 Your responsibilities:
• Develop and review documents and reports for the clinical parts of regulatory submissions
• Coordinate cross functional teams and liaise with CROs throughout clinical trials in order to ensure alignment and compliance to the company’s goals and necessary regulations
• Prepare, organise and interpret clinical data
• Support the development of clinical strategy for the company for various projects as they arise
• Manage relevant timelines required by the internal teams and external bodies from a clinical perspective
• Write CERs, clinical protocols, clinical data reports and more

🔹 Your qualifications:
• Scientific Background
• Minimum 2 years experience in a similar position within Medical Devices industry
• In-depth knowledge of regulations and standards/guides associated with clinical investigations/assessments
• Experience in writing Clinical Evaluation Report for a Medical Devices

✉️ If you are interested in this exciting role, please send your application directly to [email protected]

📲 Would you like to find out more about our open opportunities? Visit https://www.elemed.eu/vacancies/

Please note: Only candidates meeting the requirements set out in the role profile above, will be considered in the application process.

Due to the high volume of applications we receive, our team might not be able to contact each applicant individually regarding the status of their application. If you do not hear from us after 10 days, please consider your application unsuccessful.

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Elemed is Europe’s leading MedTech technical recruiter. We serve within the Medical device, diagnostic and combination device arena, working with Managers up to VP of Quality and Regulatory. Our team helps medical device experts of today become leaders of tomorrow.

📣 We won Best International Recruitment Agency at the Recruiter Awards 2021.

At Elemed, we recruit exceptional people that solve regulatory and compliance problems, so patients can have access to safe, innovative and life-changing Medical Devices.

⚖️ We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status
France

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