Clinical Manager - Post Market Studies

Role Overview

Contract: 12 months

Location: Basel; 3 days onsite

This role focuses on leading and managing global post-marketing (PMS) studies, with an emphasis on observational and low-interventional research. The position supports US and international programs, working closely with Medical Affairs and cross-functional teams to ensure high-quality real-world data generation. The role involves oversight of CROs and vendors, ensuring studies are delivered efficiently, compliantly, and on time.

Responsibilities

• Lead planning and execution of observational / non-interventional studies
• Oversee CROs, vendors, budgets, and timelines
• Coordinate with Medical Affairs, Clinical, Regulatory, and other stakeholders
• Support investigator-initiated studies (IIS)
• Ensure proper patient inclusion, data collection, and drug supply
• Monitor study progress, KPIs, and reporting
• Support post-authorisation regulatory commitments

Requirements

• Experience in observational or post-marketing (PMS) studies
• Exposure to low-interventional or real-world evidence studies
• Experience working with CROs and external vendors
• Experience coordinating across Clinical, medical RA, Supply etc
• Understanding of global clinical operations (US expertise is a must have)