Part-Time Pharmaceutical / Regulatory Affairs Project Manager, remote working, outside IR35, contract job Oversight of Regulatory and Operational Activities Monitor and manage the progress of regulatory submissions, compliance tasks, and operational deliverables to ensure alignment with EU pharmaceutical standards and timelines. Track key milestones across product lifecycle activities (e.g., MAA, variations, renewals) and proactively identify risks that may impact regulatory or commercial delivery. Strategic Prioritisation Support Partner with EU Regulatory Affairs Leads and the RA Director to define and adjust priorities based on evolving regulatory requirements, product strategy, and market needs. Ensure focus remains on high-impact regulatory and operational activities, supporting teams in navigating urgent health authority requests or critical compliance issues. Cross-Functional Coordination and Communication Act as the central liaison for all deliverables-related queries across Regulatory Affairs, Pharmacovigilance, Medical Affairs, and Commercial functions. Facilitate clear and timely communication between internal and external stakeholders (e.g., health authorities, affiliates) to maintain alignment with project goals. Provide structured updates to senior leadership and stakeholders on regulatory progress, submission status, and key deliverables. Governance and Meeting Engagement Participate in monthly operational and regulatory governance meetings to review progress, resolve challenges, and align on strategic objectives. Document and track key decisions, action items, and follow-ups to ensure accountability and continuous progress.