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

EPM Ltd.; Bury; Remote; GBP 50,000 - 70,000; Full time

Job summary

A contract research organization in the United Kingdom is seeking a clinical project manager to lead global clinical trial sites, ensuring compliance with regulatory requirements. The ideal candidate will have over 5 years of experience, strong knowledge of ICH-GCP regulations, and proven ability to manage clinical operations independently.

Qualifications

• 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.

Responsibilities

• Lead and oversee global clinical trial sites, ensuring compliance with GCP.
• Serve as the primary point of contact for stakeholders, supporting site activities.
• Ensure timely and accurate documentation, data collection, and reporting.

Skills

Clinical project management

Regulatory compliance

Communication skills

Organizational skills

Risk-based monitoring

Job description

• 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.
• 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.