Assoc. Dir, Clinical Research

539

**
6-8 years clinical research experience
Direct field monitoring or management experience
Deep knowledge of gcp and clinical regulations
** The Associate Director of Clinical Research at 539 is responsible for ensuring patient safety and high-quality data in clinical trials, overseeing Clinical Quality Management activities in the respective country or cluster. Candidates should have extensive experience in clinical research, project management, and compliance with regulations. **

Job Summary

  • The role oversees all Clinical Quality Management activities within the respective country or cluster to ensure patient safety and data quality.
  • Candidates must demonstrate a solid track record in initiating, planning, and delivering complex projects with strong project management practices.
  • The position requires supporting audits, inspections, and local training activities while implementing global processes effectively.

Matching Summary

Match Score: 75

** The Associate Director of Clinical Research at 539 is responsible for ensuring patient safety and high-quality data in clinical trials, overseeing Clinical Quality Management activities in the respective country or cluster. Candidates should have extensive experience in clinical research, project management, and compliance with regulations. **

Skills & Requirements

Must-have

  • 6-8 years clinical research experience
  • Direct field monitoring or management experience
  • Deep knowledge of GCP and clinical regulations

Nice-to-have

  • Experience in Country Operations
  • Leading cross-functional teams
  • Strategic thinking and innovation

Key Requirements

  • Bachelor's Degree in relevant health care area
  • Minimum 6-8 years relevant experience
  • Demonstrated record of accomplishments in clinical trials

Work Rights

Not specified

Tailored Resume

Cover Letter