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Clinical Trial Assistant

Sun Pharma
Sun Pharma
0-2 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 Trial Assistant – Clinical Research

Company: Sun Pharma Laboratories Ltd
Location: Sun House, Mumbai, India
Experience Required: 0–2 Years
Date Posted: 8th December 2025
Business Unit: Clinical Research
Job Type: Full-Time, Permanent


About Sun Pharma

At Sun Pharma, we empower professionals to “Create your own sunshine” by providing an environment that encourages growth, ownership, and collaboration. Our culture supports continuous learning, self-drive, and teamwork, helping you thrive while making a meaningful impact on patient care and clinical research outcomes.


Key Responsibilities

Documentation & Administrative Support

  • Assist in maintaining study documentation, including protocols, case report forms (CRFs), informed consent forms (ICFs), and study reports.

  • Organize and maintain both electronic and paper-based study files to ensure accuracy and completeness.

  • Provide administrative support, including meeting scheduling, preparing minutes, and coordinating travel arrangements as needed.

Regulatory Compliance Support

  • Assist in preparing and submitting regulatory documents to Ethics Committees and other regulatory authorities.

  • Support adherence to Good Clinical Practice (GCP) guidelines and local regulatory requirements throughout the study lifecycle.

Site Coordination & Communication

  • Assist in tracking site invoices and monitoring payment processes.

  • Perform vendor code generation and maintain accurate tracking of vendors involved in clinical trials.


Job Requirements

Educational Qualification

  • Bachelor’s or Master’s degree in Biology, Chemistry, Nursing, Pharmacy, Public Health, or related health sciences.

  • Post-graduate Diploma in Clinical Research is an added advantage.

Experience

  • 0–2 years of relevant experience in clinical research, clinical trial administration, or regulatory support.

Skills & Competencies

  • Strong organizational and administrative skills.

  • Basic understanding of clinical trial processes and regulatory requirements.

  • Effective communication and coordination skills for working with internal and external stakeholders.

  • Proficiency in MS Office and electronic documentation systems.


Why Join Sun Pharma?

  • Gain hands-on experience in clinical research operations and regulatory compliance.

  • Exposure to end-to-end clinical trial processes in a global pharmaceutical organization.

  • Opportunity to collaborate with cross-functional teams including Clinical Research, Regulatory Affairs, and Medical Affairs.

  • Structured environment for career development and professional growth.