Senior Clinical Project Manager
Excelya · Paris, France · Full-time
Description
We are seeking an experienced Clinical Project Manager to oversee and coordinate clinical activities in pharmaceutical environment. The role involves managing operational aspects of clinical trials, ensuring compliance with regulatory requirements, and acting as the primary interface between local stakeholders, investigators, vendors, and global teams. This position requires strong autonomy, rigor, and excellent communication skills, with the ability to navigate cross‑functional environments. Key Responsibilities : 1. Study Management Lead and coordinate clinical trial activities at the local level from start‑up to close‑out. Ensure local execution of global study plans in alignment with timelines and quality standards. Serve as the key point of contact for local investigational sites and regional stakeholders. 2. Regulatory & Compliance Oversight Ensure that clinical trial activities comply with local regulations, ICH‑GCP, and internal SOPs. Coordinate local submissions to competent authorities and ethics committees when required. Monitor adherence to regulatory timelines and manage any corrective actions. 3. Site & Vendor Coordination Support site selection, activation, moni…
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Questions about this job
Where is this Senior Clinical Project Manager job located?
The listing places this job in Paris, France.
Who is hiring?
The employer shown on the listing is Excelya.
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The listing does not state a salary. Ask the employer about pay, overtime and payment dates before accepting.
Is it full-time or part-time?
The listing type is Full-time.
When was this job posted?
It was posted on 8 October 2026. Jobs that stay open too long are closed automatically, so apply soon if you are interested.
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