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Associate Analyst - Clinical Trial Supply

2-7 years
Not Disclosed
10 July 29, 2025
Job Description
Job Type: Full Time Education: Master’s degree 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, India | Job Type: Full-Time | Experience: 2 to 7 Years


Job Summary

Join a leading global healthcare and life sciences innovator as an Associate Analyst – Clinical Trial Supply based in Bangalore. This dynamic role supports the end-to-end clinical supply chain, ensuring compliance with GMP and GCP standards. Ideal for candidates with a postgraduate degree in Life Sciences, MPharm, or Biotechnology and 2–7 years of experience in clinical supply coordination, documentation, and operational support within global trial environments.


Key Responsibilities

  • Support planning, scheduling, and budgeting for clinical supply projects

  • Archive and manage clinical supply documentation per GMP and GCP standards

  • Compile and control regulatory and supply documents for approval

  • Validate technical content and annexes in contracts and manage document lifecycle

  • Assist in post-trial analysis and process optimization initiatives

  • Oversee budget controls, invoice approvals, and contract preparation

  • Ensure traceability of investigational medicinal products, returns, and destruction

  • Collaborate with Clinical Supply Managers on project execution and reporting


Required Skills & Qualifications

  • Postgraduate degree in Life Sciences, Biotechnology, or MPharm

  • 2 to 7 years of experience in clinical trial supply or regulatory operations

  • Familiarity with GMP/GCP guidelines and clinical documentation practices

  • Strong organizational and document control skills

  • Excellent attention to detail and ability to manage multiple projects

  • Ability to work collaboratively across departments and timelines

  • Experience with clinical databases, KPIs, and eTMF operations is an advantage


Perks & Benefits

  • Global exposure across multiple clinical trial supply functions

  • Opportunity for career growth in a science-driven, innovative environment

  • Inclusive and flexible workplace supporting professional development

  • Empowering work culture focused on diversity and excellence

  • Join a mission-driven team impacting patients' lives worldwide


Company Description

This opportunity is with a globally renowned healthcare and life sciences company operating across healthcare, life science, and electronics. Known for innovation and inclusivity, they deliver solutions that improve, prolong, and protect lives, with teams across six continents collaborating to drive therapeutic breakthroughs in oncology, neurology, and fertility.


Work Mode:

On-site – Bangalore, India


Salary / Compensation Range:

Not disclosed in the description.


Call-to-Action

Are you ready to power the future of clinical trials and global patient care?
Apply today and bring your scientific expertise to a team redefining healthcare innovation.