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Clinical Research Associate (Clinical Trials)

Sun Pharma
Sun Pharma
1-5 years
Not Disclosed
10 Jan. 9, 2026
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

Job Title: Clinical Research Associate (CRA) – Clinical Trials
Company: Sun Pharma Laboratories Ltd
Business Unit: Clinical Research
Location: Hyderabad, India
Posted Date: December 27, 2025

Company Overview:
Sun Pharma is committed to helping employees “Create Your Own Sunshine” by fostering an environment that encourages growth, ownership, and collaboration. With a global footprint in the pharmaceutical industry, Sun Pharma empowers its workforce to innovate, lead, and thrive in a supportive and inclusive community.

Position Overview:
We are seeking a motivated Clinical Research Associate (CRA) with 1–5 years of experience in clinical research to manage and oversee clinical trials. The ideal candidate will have hands-on expertise in site management, regulatory compliance, and monitoring activities across Phase III and Phase IV clinical trials.

Key Responsibilities:

  • Conduct site feasibility assessments and identify potential investigators.

  • Negotiate study budgets, finalize investigator and site selection, and execute Confidentiality Disclosure Agreements (CDA) and study-related contracts.

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

  • Oversee investigational product (IP) dispensing, inventory management, and reconciliation.

  • Ensure timely site initiation, monitoring, and close-out activities, with accurate reporting.

  • Train investigators and site personnel on study protocols, procedures, and Good Clinical Practice (GCP) principles.

  • Monitor timely recruitment of trial participants, accurate data entry, source data verification, and query resolution.

  • Ensure timely reporting of Serious Adverse Events (SAEs) and Suspected Unexpected Serious Adverse Reactions (SUSARs) in compliance with regulatory guidelines and Sun Pharma’s pharmacovigilance policies.

  • Identify risks, analyze issues, and implement Corrective and Preventive Actions (CAPA) for underperforming sites.

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

Educational Requirements:

  • Bachelor’s or Master’s degree in Health or Life Sciences (Biology, Chemistry, Nursing, Pharmacy, Public Health) or Postgraduate Diploma in Clinical Research.

Experience Requirements:

  • Minimum 1–5 years of relevant experience in clinical research, with demonstrated expertise in site management and monitoring.

Additional Skills & Knowledge:

  • Thorough understanding of Good Clinical Practice (GCP) and regulatory guidelines for clinical trials.

  • Expertise in Phase III and Phase IV clinical trials.

  • Strong collaboration and communication skills to work effectively with cross-functional teams.

  • Ability to manage multiple sites, timelines, and deliverables efficiently.

Why Join Sun Pharma:
At Sun Pharma, your growth and success are our priorities. We provide competitive benefits, career development opportunities, and a culture of collaboration and innovation. Join us to make a meaningful impact in clinical research and contribute to improving patient outcomes globally.

Apply Today:
If you are a results-driven professional with experience in clinical research and site management, apply now to join Sun Pharma as a Clinical Research Associate (CRA) in Hyderabad.