Clinical Project Manager
We are supporting a medical devices–focused organization, operating in clinical research services, with the hiring of a Clinical Project Manager.
This is an opportunity to take ownership of clinical studies end-to-end, with strong exposure to regulatory-driven clinical research and clear career development potential.
Main Responsibilities
* Manage assigned clinical studies to ensure delivery on time and in line with agreed objectives
* Act as main point of contact for investigators, monitors, sponsors, and external partners
* Coordinate clinical trial documentation to support study submissions
* Support the drafting of clinical study documents (protocols, informed consent, CRFs)
* Prepare, maintain, and update the Trial Master File (TMF)
* Organize monitoring visits and review monitoring reports
* Coordinate site activation and oversee study conduct at clinical sites
* Coordinate data management activities, including query management
* Ensure GCP compliance throughout study execution
* Support audit and inspection activities and manage follow-up actions
Key Criteria
* Experience in clinical research within medical devices and/or pharmaceuticals
* Experience managing or coordinating clinical studies
* Knowledge of EU MDR (Regulation 2017/745)
* Hands‑on experience working in GCP‑compliant clinical trials
* Experience maintaining Trial Master File (TMF) documentation
* Fluent in English, written and spoken
Nice to have:
* CRO experience
* Experience with multi‑site or international studies
* Science‑related degree (e.g. life sciences, biotechnology, pharmaceuticals)
If this sounds like something you’d like to explore, feel free to reach out directly for a chat and share your CV.
📧 f.signorello@panda-int.com
📞 +31 (0)20 20 44 502
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