Senior Clinical Project Manager

Qmed Consulting A/S is a full‑service Contract Research Organisation (CRO) and strategic consulting partner specialising in medical devices. Based in Copenhagen and working across Europe, we are a multicultural, open‑minded, and flexible organisation dedicated to supporting manufacturers on their pathway to bring innovative medical technologies to market to enable better health. About the Role We are seeking an experienced Senior Clinical Project Manager (SCPM) to lead and manage clinical investigations within the medical device sector. You will liaise directly between Qmed functions and assigned clients, acting as that accountable point for delivery and quality whilst maintaining financial control. Typically assigned to two projects or a program, responsibilities might include managing multiple internal and external stakeholders, ensuring strong documentation practices, risk identification and implementation of mitigation strategies, and driving continuous improvement. Studies managed at this level are typically of moderate to high complexity. As a senior member of the project management team, you will play a central role in maintaining team spirit, supporting cross‑functional communication, and mentoring colleagues, while contributing to identifying and developing improved ways of working. Key Responsibilities Oversee the planning, execution, and close‑out of clinical investigations. Ensure delivery of study milestones, timelines, budgets, and quality targets. Maintain high standards of documentation and regulatory compliance. Guide and mentor project team members, fostering a collaborative and effective working environment. Proactively identify study risks and implement appropriate mitigation strategies. Work closely with internal departments to ensure alignment and efficient project delivery. Support improvements to processes, procedures, and internal best practices. Provide clear communication to clients, colleagues, and senior management. Qualifications University degree in life sciences or equivalent. At least five years of experience in clinical project management, covering all stages of trial execution. Demonstrated experience in medical device clinical investigations. In‑depth knowledge of ICH‑GCP, ISO 14155, and the Medical Device Regulation (MDR). Strong organisational skills, attention to detail, and the ability to prioritise effectively. Excellent written and verbal communication skills. Ability to build trust and motivate teams in a dynamic and evolving environment. A proactive approach paired with clear and confident presentation abilities. Professional fluency in written and spoken English. Why Join Qmed Consulting? Work within a multicultural, well‑integrated European team. Contribute directly to Qmed’s mission to enable better health. Engage in meaningful, challenging clinical projects with real impact. Join a company that values independent thinking, evidence‑based decision‑making, and genuine ownership of work. Collaborate with professionals who are committed to excellence and continuous improvement. Interested? If this opportunity aligns with your skills and aspirations, we would be pleased to hear from you. Contact For any questions regarding the position or the work we do at Qmed Consulting, please reach out to our VP of Clinical Affairs, Stephanie John, or our COO, Victoria Cavendish, Start Date As soon as possible — but we are willing to wait for the right candidate. Seniority Level Mid‑Senior level Employment Type Full‑time Job Function Project Management and Information Technology Industries Medical Equipment Manufacturing #J-18808-Ljbffr