Company: Sun Pharma Laboratories Ltd
Location: Mumbai, India (Sun House – Corporate Office)
Job Type: Full-Time
Date Posted: April 14, 2026
Experience Required: 3–5 Years (Not suitable for freshers)
About the Company
Sun Pharma Laboratories Ltd is one of the leading global pharmaceutical companies, known for delivering high-quality, affordable medicines across multiple therapeutic areas. With a strong presence in clinical research and medical affairs, the organization provides a dynamic environment for professionals aiming to build impactful careers in drug development and clinical trials.
Job Overview
We are hiring an experienced Clinical Research Associate (CRA) to manage and execute clinical trials across interventional, non-interventional, and epidemiological studies. This role offers exposure to both CRO-managed and in-house clinical studies, ensuring compliance with regulatory standards, data integrity, and patient safety.
Key Responsibilities
CRO-Managed Clinical Trials:
Manage Contract Research Organizations (CROs) for efficient study execution
Identify investigators and clinical trial sites in collaboration with internal teams
Prepare and review regulatory documents for Ethics Committee (EC) and DCGI submissions
Ensure vendor management compliance as per company policies
Coordinate clinical trial agreements and budgets with sites and CROs
Oversee regulatory submissions in coordination with Medical, Regulatory, and QA teams
Ensure proper handling, procurement, and dispatch of investigational products
Monitor and ensure timely reporting of SAEs and SUSARs
Train CRO partners on Pharmacovigilance (PV) practices
In-House Clinical Trials:
Conduct site feasibility and investigator selection
Manage study budgets, contracts, and Confidential Disclosure Agreements (CDAs)
Plan and execute Investigator Meetings
Prepare and submit documents for Ethics Committee approvals
Coordinate investigational product supply and accountability
Perform site initiation, monitoring, and close-out visits
Train site staff on protocol, GCP, and study procedures
Ensure patient recruitment targets and data quality standards are met
Conduct source data verification, CRF review, and compliance checks
Identify risks, deviations, and implement CAPA strategies
Lead data query resolution with sites and data management teams
Manage trial budgets and financial tracking
Educational Qualification
Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Nursing, or related field
Postgraduate Diploma in Clinical Research is preferred
Required Experience & Skills
3–5 years of experience in Clinical Research within Pharma, CRO, or Biotech organizations
Strong experience in multi-site clinical trial management
Knowledge of risk-based and remote monitoring methodologies
Experience handling audits and regulatory inspections
In-depth understanding of ICH-GCP, New Drugs and Clinical Trial Rules (2019), ICMR Guidelines (2017), and Drugs & Cosmetics Act
Strong research methodology and clinical trial design knowledge
Ability to work in matrix and cross-functional environments
Excellent analytical, communication, and stakeholder management skills
Core Competencies
Integrity-driven decision making
Strong clinical research and operational expertise
Strategic thinking with attention to detail
High accountability and performance-driven mindset
Effective collaboration in cross-functional teams
Adaptability and problem-solving capabilities
Work Environment & Travel
This is primarily an office-based role in Mumbai, with approximately 8–10 days of travel per month for site visits and monitoring activities.
Important Note for Applicants
This position requires prior hands-on experience in clinical trial operations and monitoring. Freshers are encouraged to apply for entry-level roles such as Clinical Trial Assistant (CTA) or Junior CRA before progressing to this level.
How to Apply
Candidates can apply through the official careers page of Sun Pharma Laboratories Ltd or explore verified global clinical research opportunities on ThePharmaDaily.com.
Disclaimer
This job description outlines the general responsibilities and expectations for the role. The organization reserves the right to modify duties based on business requirements and operational needs.
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