In this client-facing consulting role, as part of the clinical team you will take full responsibility for the setup and operational management of clinical investigations on behalf of our clients in the medical device and IVD sectors.
At regenold, we work in a client-focused environment that is dynamic and responsibility-driven.
If you are someone who enjoys taking ownership, guiding and advising clients with confidence and managing projects independently, this role is for you.
If you prefer purely procedural or methodical work, this role may not be for you..
Your main tasks will include:
- Taking responsibility for the setup and operational delivery of clinical investigations for regenold clients in the medical device and IVD field
- Selecting, qualifying, and overseeing CROs and other external vendors, including feasibility, budget negotiations, contracting and performance management
- Sponsor oversight activities to ensure study quality, compliance and timely execution
- Preparing and submitting Clinical Trial Applications and managing requests and deficiency communications
- Driving cross-functional stakeholder communication and ensuring effective study governance structures
- Managing clinical investigations end to end, from study planning to close-out
- Reviewing key study documentation, including CRO monitoring outputs and deviations, ensuring documentation quality throughout the project
