Clinical Lead Project Manager
PSI CRO · France
Clinical Research
Remote/Hybrid — check advert
Not yet analysed
Demand80
Career growth76
Healthcare fit74
Remote potential80
5-year outlook
Experienced CRO clinical project managers generally see stable demand and compensation growth as they manage larger global studies, deepen oncology/GI therapeutic experience, and take on more client-facing responsibilities. Actual pay varies by country, CRO, and seniority.
Clinical license
Not required
Applicant reach
narrow
Seniority
senior
Employment type
full-time
Date found
2026-10-29
Intelligence details
Flexible work details
- Engagement type
- Contract
- Hours
- Variable hours
- Rate period
- Annual
Why this was classified this way
- Contract
Listing via Himalayas.
Eligibility, licensing, and location restrictions can change. Always confirm details on the source posting before applying.
Why this is worth applying to
Worth applying for clinicians who already have CRO, sponsor, or site-level clinical trial management experience and want a non-bedside, client-facing leadership role. Clinicians without clinical research project management experience should build that background first.
Who should apply
Experienced clinical research professionals, especially doctors, nurses, pharmacists, or allied health professionals with CRO, sponsor, or site trial management experience in Phase II/III studies and oncology/GI/IBD therapeutic areas.
CV angle
Foreground real clinical trial and project management work: multi-site coordination, startup-to-closeout support, protocol and GCP compliance, budget/timeline tracking, cross-functional team leadership, vendor/client communication, and therapeutic experience. Translate clinical leadership, audit, and quality/compliance work into project management language, but do not claim PM titles or CRO/sponsor experience you do not have.
Skills to highlight
- Clinical trial project management
- Global/multi-center study coordination
- Phase II/III trial delivery
- Budget and timeline management
- Cross-functional team leadership
- Client and stakeholder communication
- GCP/regulatory compliance
- Oncology/GI/IBD therapeutic experience
Role summary
Lead global, multi-center clinical research projects from startup to closure, managing timelines, budgets, teams, clients, proposals, and compliance for a contract research organization.
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