Freelance - Clinical Project Manager (0.8 FTE) (Remote)

Freelance - Clinical Project Manager (0.8 FTE) (Remote)

Start Date: 2026-09-26T00:00:00

Location: Altrincham, Greater Manchester, GB, WA14 1

End Date: 2026-12-30T03:01:49.52

Altrincham

About the Role

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 to you, please apply directly.

#s1-Gen

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.