Freelance - Clinical Project Manager (0.8 FTE) (Remote)
Posted 1 week ago by EPM Scientific
Negotiable
Undetermined
Remote
England, United Kingdom
Summary: EPM Scientific is seeking a Freelance Clinical Project Manager to support upcoming Oncology Trials in the EU. The role involves leading global clinical trial sites and ensuring compliance with regulatory requirements. The position is remote and requires a commitment of 0.8 to 1 FTE for a 12-month contract. Candidates should have significant experience in clinical project management, particularly in Oncology.
Key Responsibilities:
- Lead and oversee global clinical trial sites, ensuring compliance with GCP, protocol, and regulatory requirements.
- Serve as the primary point of contact for internal and external stakeholders, supporting site initiation, monitoring, and close-out activities.
- Ensure timely and accurate documentation, data collection, and reporting in line with project timelines.
- Collaborate with cross-functional teams including CRAs, Medical Monitors, Regulatory Affairs, and Data Management.
- Contribute to risk-based monitoring strategies and support audit readiness.
Key Skills:
- 5 years+ experience in clinical project management, preferably in Oncology.
- Strong knowledge of ICH-GCP and EMA & FDA regulatory environment.
- Proven ability to work independently and manage global clinical operations.
- Excellent communication and organizational skills.
- Eligibility to work as a Freelancer in your country of residence.
Salary (Rate): undetermined
City: England
Country: United Kingdom
Working Arrangements: remote
IR35 Status: undetermined
Seniority Level: undetermined
Industry: Other
EPM Scientific are currently partnered with a Biotechnology company who are seeking a Freelance Clinical Project Manager to support their upcoming Oncology Trials in the EU. See a short summary below:
Contract Conditions:
- Start date: ASAP
- Location: European Union (Remote)
- Contract: 0.8 - 1 FTE, 12-Month Contract
- Project: Oncology - Phase 3 Global Trial
Key Responsibilities:
- Lead and oversee global clinical trial sites, ensuring compliance with GCP, protocol, and regulatory requirements.
- Serve as the primary point of contact for internal and external stakeholders, supporting site initiation, monitoring, and close-out activities.
- Ensure timely and accurate documentation, data collection, and reporting in line with project timelines.
- Collaborate with cross-functional teams including CRAs, Medical Monitors, Regulatory Affairs, and Data Management.
- Contribute to risk-based monitoring strategies and support audit readiness.
Requirements:
- 5 years+ experience in clinical project management, preferably in Oncology.
- Strong knowledge of ICH-GCP and EMA & FDA regulatory environment.
- Proven ability to work independently and manage global clinical operations.
- Excellent communication and organizational skills.
- Eligibility to work as a Freelancer in your country of residence.
If the role is of interest of you, please apply directly.