Clinical Research Associate – Clinical Trials
Company: Sun Pharma Laboratories Ltd
Location: Hyderabad, India
Experience Required: 1–5 Years
Date Posted: 27th December 2025
Business Unit: Clinical Research
Job Type: Full-Time, Permanent
About Sun Pharma
At Sun Pharma, we empower our employees to “Create your own sunshine” by fostering a culture of growth, collaboration, and continuous learning. We encourage self-driven professionals to take charge of their career journeys, work with confidence, and thrive in a supportive environment.
Key Responsibilities
Site & Investigator Management
Conduct site feasibility assessments and identify potential investigators for clinical trials.
Negotiate study budgets with investigators and finalize site selection, Confidentiality Disclosure Agreements (CDA), and study contracts.
Coordinate site initiation, monitoring, and close-out activities, ensuring all reports are completed and submitted on time.
Train investigators and site personnel on study protocols, procedures, and Good Clinical Practice (GCP) principles.
Clinical Trial Oversight
Manage Investigational Product (IP) dispensing, inventory, and reconciliation.
Oversee timely recruitment of trial participants, data entry, source data verification, and query resolution.
Ensure adverse event reporting (SAEs, SUSARs) in alignment with regulations and Sun Pharma’s Pharmacovigilance policies.
Identify site risks, analyze issues, and implement Corrective and Preventive Actions (CAPA) as needed.
Cross-Functional Coordination
Collaborate with in-house or CRO partners for data management, statistical analysis, and database lock (DBL).
Support preparation and submission of Ethics Committee (EC) documents across multiple centers.
Maintain regular communication with cross-functional stakeholders to ensure study timelines and quality standards are met.
Required Qualifications & Skills
Education: Bachelor’s or Master’s degree in Pharmacy, Nursing, Biology, Chemistry, Public Health, or a Postgraduate Diploma in Clinical Research.
Experience: 1–5 years of relevant experience in clinical research, preferably in Phase III/IV clinical trials.
Strong understanding of GCP, regulatory guidelines, and clinical trial processes.
Proven expertise in site management, investigator coordination, and cross-functional collaboration.
Excellent communication, documentation, and organizational skills.
Why Join Sun Pharma?
Opportunities for personal and professional growth within a global pharmaceutical leader.
Exposure to advanced clinical trial operations and regulatory compliance standards.
Collaborative, supportive, and innovation-driven work culture.
Contribute directly to advancing healthcare solutions and patient outcomes.
At Sun Pharma, every day is an opportunity to grow, collaborate, and make a meaningful impact in the lives of patients globally.
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