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Clinical Research Associate

Sun Pharma
2-5 years
INR 5 LPA – 9 LPA
Mumbai, India
1 June 24, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Clinical Trials, Detail-Oriented, Drug Development, Lifesciences, Negotiation Skills, Regulatory Compliance

CLINICAL RESEARCH ASSOCIATE

Company: Sun Pharma Laboratories Ltd
Business Unit: Clinical Research
Location: Mumbai

JOB OVERVIEW

Sun Pharma is seeking a Clinical Research Associate (CRA) to support the planning, execution, monitoring, and management of clinical trials. The role involves coordinating with investigators, clinical sites, CROs, ethics committees, and internal stakeholders to ensure studies are conducted in compliance with GCP, regulatory requirements, and company policies.

KEY RESPONSIBILITIES

  • Perform site feasibility assessments and identify potential investigators.

  • Negotiate study budgets with investigators and finalize study sites.

  • Execute Confidentiality Disclosure Agreements (CDAs) and study-related contracts.

  • Prepare and submit study-related documents for Ethics Committee (EC) approvals across study centers.

  • Oversee and document Investigational Product (IP) dispensing, inventory management, accountability, and reconciliation.

  • Ensure timely site initiation, routine monitoring, and close-out visits.

  • Generate and maintain monitoring reports and site documentation.

  • Conduct investigator and site personnel training on study protocols, procedures, and Good Clinical Practice (GCP) guidelines.

  • Support timely recruitment and retention of study participants.

  • Ensure efficient source data verification (SDV), data entry review, and query resolution.

  • Ensure timely reporting of Serious Adverse Events (SAEs) and Suspected Unexpected Serious Adverse Reactions (SUSARs) according to regulatory requirements and Sun Pharma Pharmacovigilance policies.

  • Identify site-related risks and implement corrective and preventive actions (CAPA) when performance issues arise.

  • Coordinate with CROs and internal teams for data management, database lock (DBL), statistical analysis, and study reporting activities.

EDUCATIONAL QUALIFICATIONS

  • Bachelor’s or Master’s Degree in:

    • Biology

    • Chemistry

    • Nursing

    • Pharmacy

    • Public Health

    • Life Sciences or related healthcare field

OR

  • Post Graduate Diploma in Clinical Research

EXPERIENCE

  • Minimum 2–5 years of relevant experience in Clinical Research.

  • Experience in clinical trial monitoring and site management.

  • Experience in Phase III and Phase IV Clinical Trials preferred.