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Clinical Research Associate (Clinical Trials)

Sun Pharma
Sun Pharma
1-5 years
Not Disclosed
10 Dec. 29, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences 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

Clinical Research Associate – Clinical Trials

Company: Sun Pharma Laboratories Ltd
Location: Hyderabad, India (Sun House – Corporate Office)
Experience Required: 1–5 Years
Date Posted: 6th December 2025
Business Unit: Clinical Research
Job Type: Full-Time, Permanent


About Sun Pharma

At Sun Pharma, we are committed to helping you “Create your own sunshine” by fostering an environment that promotes growth, self-drive, and collaboration. We provide a supportive culture where professionals can take charge of their careers, continuously improve, and thrive in a dynamic, high-performing environment.


Key Responsibilities

Site & Investigator Management

  • Conduct site feasibility assessments and identify potential investigators.

  • 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 timely completion and submission of required reports.

  • Train investigators and site personnel on study protocols, procedures, and GCP principles.

Clinical Trial Oversight

  • Manage Investigational Product (IP) dispensing, inventory management, and reconciliation.

  • Ensure efficient participant recruitment, data entry, source data verification, and query resolution.

  • Facilitate timely reporting of SAEs, SUSARs, and ensure compliance with Sun Pharma’s Pharmacovigilance policies.

  • Identify site risks, perform analyses, and implement Corrective and Preventive Actions (CAPA) as required.

Cross-Functional Collaboration

  • Coordinate with in-house teams or CRO partners for data management, statistical analysis, statistical reports, and database lock (DBL).

  • Prepare and submit Ethics Committee (EC) documents for multi-center trials.

  • Maintain strong communication with cross-functional stakeholders to ensure study timelines and quality standards are consistently met.


Required Qualifications & Skills

  • Education: Bachelor’s or Master’s degree in Pharmacy, Nursing, Biology, Chemistry, Public Health, or Postgraduate Diploma in Clinical Research.

  • Experience: 1–5 years of experience in clinical research, preferably in Phase III and Phase IV clinical trials.

  • Strong knowledge of GCP practices, regulatory guidelines, and clinical trial processes.

  • Expertise in site management and investigator coordination.

  • Proven ability to collaborate across functional teams and maintain high-quality documentation.

  • Excellent communication, analytical, and organizational skills.


Why Join Sun Pharma?

  • Exposure to advanced clinical research operations and regulatory compliance standards.

  • Opportunities for personal and professional growth in a global pharmaceutical leader.

  • Supportive and collaborative work environment with impactful career development opportunities.

  • Contribute directly to improving patient outcomes and advancing healthcare solutions globally.

At Sun Pharma, each day is an opportunity to grow, collaborate, and make a meaningful impact in the lives of patients worldwide.