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.
* Eligibilty to work as a Freelancer in your country of residence.
If the role is of interest of you, please apply directly.