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A leading medical device company based in Paris are seeking an experienced Clinical Project Manager to join their team. The successful candidate will be responsible for managing a Cardiology Medical Device clinical trial. Candidate should be available for a fixed term contract (12 months), 40 hours per week.
Responsibilities:
* Manage the overall conduct of clinical trials, including CRA management and CRO oversight
* Ensure that trials are conducted in compliance with regulatory requirements and company standards
* Ensure that all trial-related documentation is accurate, complete and maintained in accordance with company standards
* Ensure that all trial-related activities are conducted within budget and timelines
* Work closely with cross-functional teams including R&D, Regulatory, Medical Affairs and Marketing
* Provide regular updates to senior management on trial progress, risks and issues
* Work with external vendors and suppliers to ensure that trial-related activities are delivered on time and to the required quality standards
Requirements:
* Must be Paris Based, available to work in the office
* Medical device experience in clinical research industry essential
* Cardiology experience preferred but not essential
* Must have experience working directly with US sites
* French language preferred but not essential
If you are an experienced Clinical Project Manager with experience with Medical devices, please submit your CV for consideration.
Clinical Project Manager
- Location Paris
- Job type Contract
- Salary Negotiable
- Discipline Clinical Operations
- Reference CR/412874_1679328593
Responsibilities:
* Manage the overall conduct of clinical trials, including CRA management and CRO oversight
* Ensure that trials are conducted in compliance with regulatory requirements and company standards
* Ensure that all trial-related documentation is accurate, complete and maintained in accordance with company standards
* Ensure that all trial-related activities are conducted within budget and timelines
* Work closely with cross-functional teams including R&D, Regulatory, Medical Affairs and Marketing
* Provide regular updates to senior management on trial progress, risks and issues
* Work with external vendors and suppliers to ensure that trial-related activities are delivered on time and to the required quality standards
Requirements:
* Must be Paris Based, available to work in the office
* Medical device experience in clinical research industry essential
* Cardiology experience preferred but not essential
* Must have experience working directly with US sites
* French language preferred but not essential
If you are an experienced Clinical Project Manager with experience with Medical devices, please submit your CV for consideration.