Merck & Co., Inc. is seeking an Associate Director for Clinical Research to oversee Clinical Quality Management (CQM) activities. The ideal candidate will have significant experience in clinical research, project management, and a strong understanding of clinical trial regulations
Job Summary
The role is critical for ensuring patient safety, high-quality data, and regulatory compliance across all clinical trials.
Under the guidance of the Regional Director, the position oversees all Clinical Quality Management activities in the respective country or cluster.
Candidates must demonstrate a solid track record in initiating projects, leading cross-functional teams, and supporting continuous improvement initiatives.
Matching Summary
Match Score: 85
Merck & Co., Inc. is seeking an Associate Director for Clinical Research to oversee Clinical Quality Management (CQM) activities. The ideal candidate will have significant experience in clinical research, project management, and a strong understanding of clinical trial regulations.
Skills & Requirements
Must-have
6-8 years clinical research experience
Direct field monitoring or management experience
Deep knowledge of GCP and clinical regulations
Project management and cross-functional team leadership
Nice-to-have
Experience in Country Operations
Quality Control Activities and Process Improvement
Experience managing audits and inspections
Coordinating and delivering training sessions
Key Requirements
Bachelor's Degree in relevant health care area
Minimum 6-8 years relevant clinical research experience
Demonstrated record of accomplishments in clinical trials