What you can expect

• Direct the conduct of the trial in collaboration with the Principal Investigator and Steering Committee, ensuring adherence to protocol and regulatory requirements
• Coordinate and participate in patient and public involvement activities
• Train and support site personnel in protocol procedures and data capture
• Organize and document screening, enrolment, follow-up, and study visits
• Act as central contact for Ethics Committees, Competent Authorities, investigators, study nurses, and participants
• Ensure high-quality data collection, perform QC checks, and coordinate resolution of data queries
• Support and monitor recruitment strategies to optimize enrolment
• Report serious and unexpected adverse events to the Sponsor-Investigator and regulatory agencies
• Organize and participate in monitoring visits and audits

Your Profile

• Strong interest in patient-oriented research
• Proven experience in clinical studies, with solid knowledge of GCP, Swiss Ethics Committee processes, and regulatory requirements
• Excellent organizational skills, reliability, and attention to detail
• Strong interpersonal and communication skills
• Fluency in German and English; good knowledge of French and Italian will be an advantage
• Ability to work independently while coordinating across multiple national and international sites
• Advantage: experience in leading multicentre studies and/or a CAS/DAS in Clinical Study Management

What we offer

• A highly stimulating and collaborative academic environment
• The opportunity to shape and coordinate a multinational SNSF-funded clinical trial with direct impact on patient care
• An interdisciplinary working culture with excellent opportunities for professional growth
• Salary according to SNSF guidelines