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.