PHARMA BHARAT
PHARMACEUTICAL JOB PORTAL
No new notifications

Ad

Sun Pharma Hiring Clinical Research Associates for Mumbai & Delhi

Published on

Sun Pharma Laboratories Ltd

B.Pharm, M.Pharm, Pharm.D, Msc, BSc, Lifesciences, Biology, Chemistry, Nursing, Public Health, or related,Diploma in Clinical Research

Mumbai, Delhi

1 - 5 Years

Verified Job

Online Application
Ad

Sun Pharma Laboratories Ltd is inviting applications for the position of Clinical Research Associate (CRA) in Mumbai and Delhi under its Medical Affairs & Clinical Research division. This opportunity is ideal for professionals with 1โ€“5 years of clinical research experience who are looking to build a rewarding career in clinical operations, site monitoring, GCP compliance, and investigator management.

If you have experience in clinical trial monitoring, site management, ethics committee submissions, GCP, SAE reporting, and clinical research operations, this Sun Pharma Clinical Research Associate job offers an excellent opportunity to work with one of India’s leading pharmaceutical companies.


Job Details

  • Position: Clinical Research Associate (CRA)
  • Company: Sun Pharma Laboratories Ltd
  • Business Unit: Medical Affairs & Clinical Research
  • Locations:
    • Mumbai
    • Delhi
  • Job Type: Full-Time
  • Experience: 1โ€“5 Years
  • Date Posted: August 4, 2026

Key Responsibilities

As a Clinical Research Associate at Sun Pharma, you will:

  • Perform site feasibility assessments and identify suitable investigators.
  • Negotiate study budgets with investigators and clinical sites.
  • Execute Confidentiality Disclosure Agreements (CDA) and study-related contracts.
  • Prepare and submit documents for Ethics Committee (EC) approvals.
  • Manage Investigational Product (IP) dispensing, inventory, and reconciliation.
  • Conduct Site Initiation Visits (SIV), Monitoring Visits (MV), and Close-Out Visits (COV).
  • Train investigators and site staff on study protocols and Good Clinical Practice (GCP).
  • Monitor patient recruitment and ensure timely data collection.
  • Perform Source Data Verification (SDV) and resolve data queries.
  • Ensure timely reporting of SAEs and SUSARs in compliance with regulations and Sun Pharma Pharmacovigilance policies.
  • Identify study risks and implement CAPA for underperforming sites.
  • Coordinate with CROs and internal teams for:
    • Data Management
    • Statistical Analysis
    • Database Lock (DBL)
    • Clinical Study Reporting

Required Qualifications

Applicants should possess any of the following:

  • Bachelor’s Degree in Pharmacy, Biology, Chemistry, Nursing, Public Health, or related Life Sciences
  • Master’s Degree in a Health-related discipline
  • Post Graduate Diploma in Clinical Research

Experience Required

  • 1โ€“5 years of relevant Clinical Research experience.
  • Experience in site monitoring, GCP compliance, investigator management, EC submissions, and clinical trial coordination is preferred.

Preferred Skills

  • Clinical Trial Monitoring
  • GCP & ICH Guidelines
  • Site Management
  • Ethics Committee Submission
  • Source Data Verification (SDV)
  • SAE & SUSAR Reporting
  • Clinical Operations
  • Investigator Management
  • CAPA Management
  • Data Management Coordination
  • CRO Coordination
  • Excellent communication and documentation skills

Why Join Sun Pharma?

Sun Pharma offers professionals an environment focused on continuous learning and career growth.

Benefits include:

  • Career development opportunities
  • Exposure to multicenter clinical trials
  • Collaborative Medical Affairs environment
  • Opportunity to work with experienced clinical research professionals
  • Professional growth in Clinical Operations

Who Should Apply?

This opportunity is suitable for candidates with backgrounds in:

  • B.Pharm
  • M.Pharm
  • B.Sc Life Sciences
  • M.Sc Life Sciences
  • Nursing
  • Biology
  • Chemistry
  • Public Health
  • PG Diploma in Clinical Research

How to Apply

Application Link For Mumbai

Application Link For Delhi

Ad

Share This Job

โœ… Copied!