Listed on Merck’s own careers site. You apply with them directly — we never stand between you and the employer.
What this role is
This role manages clinical trial quality, regulatory compliance, and data integrity across a country's operations, ensuring patient safety and adherence to global standards. It suits experienced clinical research professionals with strong project management skills who are ready to lead cross-functional teams and navigate complex regulatory environments.
Our summary, not Merck’s wording. The full posting is on their site.
Skills this role names
Log in to see which of these are already on your profile.
What they ask for
Required
- Bachelor's degree or equivalent in a relevant healthcare field
- Minimum 6–8 years of clinical research experience including field monitoring or oversight of monitoring staff
- Deep knowledge of clinical trial processes, GCP, and clinical research regulations
- Project management experience with demonstrated track record of initiating, planning, and delivering projects
- Experience leading cross-functional teams
- Superior oral and written communication skills in an international environment
- Excellent project management, organizational, and prioritization skills
- Excellent teamwork skills including conflict resolution and discretion
Nice to have
- Experience in country operations
- Experience in clinical quality management including quality control activities
- Experience in process management and improvement
- Experience managing audits and inspections
- Experience coordinating and delivering training sessions