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Clinical Research Associate (Clinical Trials)

1-5 years
Not Disclosed
10 Nov. 10, 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

Job Title: Clinical Research Associate (Clinical Trials)
Company: Sun Pharma Laboratories Ltd
Business Unit: Clinical Research
Location: Hyderabad, India (Sun House - Corporate Office)
Date Posted: Nov 7, 2025

Company Overview:
At Sun Pharma, employees are encouraged to “Create your own sunshine” by fostering growth, self-drive, collaboration, and continuous improvement. The company emphasizes professional development, teamwork, and supportive work culture.

Role Summary:
As a Clinical Research Associate, you will oversee clinical trial site activities, ensure regulatory compliance, monitor trial progress, and support data integrity. You will collaborate with internal and external stakeholders to facilitate smooth trial execution.

Key Responsibilities:

  • Perform site feasibility assessments, identify potential investigators, negotiate study budgets, finalize sites, and execute CDAs and study-related contracts.

  • Prepare and submit study documents for EC approval across multiple centers.

  • Oversee IP dispensing, inventory management, and reconciliation.

  • Conduct site initiation, monitoring, and close-out activities and generate corresponding reports.

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

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

  • Ensure timely reporting of SAEs, SUSARs, and alignment with regulatory and Sun Pharma PV policies.

  • Identify, analyze, and implement CAPA for sites not meeting expectations.

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

Qualifications:

  • Bachelor’s or Master’s degree in a health or related field (e.g., Biology, Chemistry, Nursing, Pharmacy, Public Health) and/or Post-graduate Diploma in Clinical Research.

Experience:

  • 1–5 years of relevant experience in Clinical Research.

Skills & Competencies:

  • Knowledge of GCP practices and regulatory guidelines in clinical trials.

  • Expertise in Phase III and Phase IV clinical trials.

  • Site management expertise.

  • Ability to collaborate with cross-functional stakeholders.

Additional Information:

  • Sun Pharma provides robust benefits, professional growth opportunities, and a supportive work environment.

  • Job description may evolve; employees may be assigned comparable duties commensurate with experience.