# (Asso./Sr.) Manager/Asso. Dir, Country Clincial Quality Management

Hiring organization: [Merck](https://career.thegoodapps.co/organizations/merck)

Canonical page: https://career.thegoodapps.co/jobs/ecef1a66-6933-4587-9788-44f00bceda99

Listed on Merck's own careers site. Applications go to them directly.

- Seniority: Senior

## Summary

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._

## Skills named

Clinical Research, Clinical Trials, Data Analysis, Quality Management, Root Cause Analysis

## 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

Apply on Merck's site: https://msd.wd5.myworkdayjobs.com/en-US/SearchJobs/job/CHN---Beijing---Beijing-Wangjing-Park/XMLNAME--Asso-Sr--Manager--Country-Clincial-Quality-Management_R390642-2