Associate Analyst - Clinical Trial Supply
Location: Bangalore, Karnataka, India
Job Type: Full-Time
Company: Merck Group
Overview:
Merck is seeking an Associate Analyst – Clinical Trial Supply to support global clinical trial operations, including finance, contracts, eTMF operations, and database & KPI management. The role plays a vital part in maintaining GMP/GCP compliance, managing documentation, supporting supply projects, and driving process improvements across the Clinical Trial Supply (CTS) team.
Key Responsibilities:
Support planning, scheduling, budgeting, and resource allocation for clinical supply projects
Archive documentation in compliance with GMP and GCP requirements in internal and external systems
Ensure completeness and accuracy of technical specifications, contracts, and annexes
Assist in drafting, reviewing, and archiving project documents such as plans, reports, and meeting minutes
Help prepare supply contracts and manage the budget/invoice process within defined frameworks
Contribute to post-trial reviews and continuous process optimization
Maintain full global traceability of Investigational Medicinal Products (IMPs), including returns and destruction
Support Clinical Supply Manager and Coordinator in daily project-related activities
Candidate Profile:
Education: Postgraduate degree in Life Sciences, Biotechnology, or MPharm
Experience: 2 to 7 years in clinical trial supply or related areas
Preferred Skills:
Knowledge of GMP and GCP compliance
Strong documentation, communication, and organizational skills
Proficient in MS Office and database tools
Familiarity with budgeting, contract management, and clinical supply chain processes
Estimated Salary: ₹7–11 LPA (based on experience and industry standards)
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