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Clinical Trial Assistant

Sun Pharma
Sun Pharma
0-2 years
Not Disclosed
10 Jan. 20, 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

Clinical Trial Assistant (CTA)

Company: Sun Pharmaceutical Laboratories Ltd
Business Unit: Clinical Research
Location: Sun House – Corporate Office, Mumbai, India
Job Type: Full-Time
Posted Date: January 6, 2026
Experience Required: 0–2 Years


Job Overview

Sun Pharmaceutical Laboratories Ltd is seeking a motivated Clinical Trial Assistant (CTA) to join its Clinical Research team at the corporate office in Mumbai. This entry-level role is ideal for candidates looking to build a strong foundation in clinical research operations, regulatory documentation, and site coordination within a leading global pharmaceutical organization.

The Clinical Trial Assistant will provide essential administrative, documentation, and coordination support to ensure smooth execution of clinical trials in compliance with regulatory and Good Clinical Practice (GCP) requirements.


Key Responsibilities

Documentation and Administrative Support

  • Assist in the preparation, maintenance, and organization of essential clinical trial documents, including protocols, informed consent forms (ICFs), case report forms (CRFs), and study reports

  • Maintain electronic and paper-based Trial Master Files (TMF) ensuring accuracy, completeness, and inspection readiness

  • Provide administrative support such as scheduling meetings, preparing meeting agendas and minutes, and coordinating internal or external communications

Regulatory and Compliance Support

  • Support the preparation and submission of study-related documents to Ethics Committees (ECs) and regulatory authorities

  • Assist in maintaining compliance with ICH-GCP guidelines, local regulations, and internal SOPs throughout the study lifecycle

Site Coordination and Vendor Support

  • Assist in tracking site invoices, payment processing, and financial documentation

  • Support vendor code generation, vendor tracking, and coordination with internal finance and procurement teams

  • Facilitate effective communication between study sites, vendors, and internal clinical teams


Educational Qualification

  • Bachelor’s or Master’s degree in a health-related discipline such as Pharmacy, Life Sciences, Nursing, Biology, Chemistry, or Public Health
    OR

  • Postgraduate Diploma in Clinical Research


Experience Requirements

  • 0 to 2 years of relevant experience in Clinical Research, Clinical Operations, or Trial Support roles

  • Freshers with relevant academic training or internships in clinical research are encouraged to apply


Required Skills and Competencies

  • Basic understanding of clinical trial processes and documentation

  • Knowledge of Good Clinical Practice (GCP) and regulatory requirements

  • Strong organizational and documentation skills

  • Attention to detail and ability to manage multiple tasks simultaneously

  • Good written and verbal communication skills in English

  • Proficiency in MS Office applications

  • Ability to work collaboratively within cross-functional clinical research teams


Why Join Sun Pharma?

Sun Pharma offers a structured and supportive environment for early-career professionals to grow within the clinical research domain. Employees gain exposure to global clinical trials, regulatory processes, and industry best practices, along with opportunities for continuous learning and long-term career development.


Disclaimer

This job description outlines the general nature and level of responsibilities associated with this role. It is not intended to be an exhaustive list of duties, responsibilities, or qualifications. Sun Pharmaceutical Laboratories Ltd reserves the right to modify job responsibilities based on business requirements.