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 ADZN1_UKTJ