Clinical Project Manager Late Phase

Planet Pharma Staffing Limited; United Kingdom; Remote; GBP 60,000 - 80,000; Full time

Job description

Freelance Late Phase Clinical Project Manager – PASS / Registries

Remote based across EU & UK

Start Date: Immediate

The Role:

We are seeking an experienced Clinical Project Manager (CPM) to lead and manage late-phase and real-world evidence studies, particularly PASS and disease/product registries. This role is ideal for a hands-on, proactive leader who thrives in a collaborative environment and has a solid background in non-interventional or observational studies.

Key Responsibilities:

• Manage the planning, execution, and delivery of post-approval clinical studies (PASS, registries) in compliance with GCP, local regulations, and internal SOPs
• Act as the main point of contact for sponsors, vendors, and cross-functional teams
• Develop study documents (protocols, SAPs, CRFs, etc.) in collaboration with medical and regulatory teams
• Oversee timelines, budgets, and resources to ensure successful project delivery
• Support regulatory submissions, ethics applications, and safety reporting processes
• Ensure data quality and study compliance through robust vendor and site management
• Lead project team meetings and provide regular status updates to stakeholders
• Drive continuous improvement and lessons learned across late-phase programs

Requirements:

• Degree in life sciences or related field
• Minimum 4-5 years of clinical project management experience, with a strong focus on late-phase/post-marketing studies
• Demonstrated experience managing PASS, registries, or non-interventional studies
• Solid understanding of real-world evidence generation, GVP, and relevant regulatory frameworks (e.g., EMA PASS guidance)
• Excellent communication, leadership, and stakeholder management skills
• Experience working with CROs, vendors, and multi-country studies preferred
• Fluent in English; additional languages a plus