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Associate Analyst - Clinical Trial Supply

2-7 years
₹7–11 LPA
10 July 28, 2025
Job Description
Job Type: Full Time Education: M.Sc./M.Pharm/PhD Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

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)