About the job
Clinical Project Manager – Switzerland
Employment Type: Permanent
Chloe O’Shea is partnered with a mid-sized to large, global pharmaceutical company headquartered near Zurich, Switzerland. Known for its long-term perspective, people-focused culture, and innovative therapies, this organisation offers the best of both worlds – the resources of a global player combined with the values of a family-owned business.
This is an exciting opportunity for an experienced Clinical Project Manager to play a central role in advancing life-saving therapies across coagulation and critical care.
The Role
As a Senior Clinical Project Manager, you will lead global Phase I–IV GCP studies, ensuring high-quality execution, scientific excellence, and regulatory compliance. You will oversee multidisciplinary teams, collaborate with external partners, and represent clinical research in high-level discussions with health authorities. This role is ideal for senior professionals with a proven track record in clinical research who are looking to shape impactful development programs and contribute to therapies that make a real difference for patients.
Key Responsibilities
- Plan, implement, and oversee global clinical trials (Phases I–IV) in line with GCP requirements.
- Provide input into overall clinical development strategies and lead protocol design.
- Analyse and interpret clinical data, prepare study reports, CTDs, and expert statements for submission to competent authorities.
- Manage trial budgets and vendor oversight, ensuring timelines and quality standards are met.
- Engage with Independent Data Monitoring and Steering Committees, presenting study results and updates.
- Represent clinical research in meetings with regulatory authorities and contribute to publications and congress presentations.
- Stay up to date with the latest scientific and regulatory developments relevant to ongoing studies.
Requirements
- PhD or MD background.
- 8+ years’ experience in clinical research as a Clinical Project Manager (10+ for Senior CPM).
- Strong expertise in managing Phase I–IV trials within a pharmaceutical or biotechnology environment.
- Excellent communication, organisational, and leadership skills with the ability to inspire cross-functional teams.
- In-depth knowledge of medical terminology, physiology, and clinical trial processes.
- Experience in writing clinical protocols, procedures, and regulatory documentation.
- Background in coagulation or critical care is an advantage.
- Strong project management and problem-solving skills with proven vendor/CRO oversight experience.
- Fluent in German and English, both written and spoken.
- Willingness to travel up to 30%.
What’s in It for You?
- The opportunity to contribute directly to the development of life-saving medicines.
- A people-focused culture that combines long-term career perspective with strong family values.
- Market-competitive salary and comprehensive benefits package.
- A collaborative and supportive environment with skilled, motivated colleagues.
- Ongoing professional development through internal and external training opportunities.
Apply Today!
If you are an experienced Clinical Project Manager ready to lead global trials and make a lasting impact on patients’ lives, we would love to hear from you.
