Clinical Trial Assistant
Date Posted: January 6, 2026
Company: Sun Pharma Laboratories Ltd
Business Unit: Clinical Research
Location: Mumbai, India
Work Location: Sun House – Corporate Office
Employment Type: Full-time
About Sun Pharma
Sun Pharma Laboratories Ltd is a globally recognized pharmaceutical organization committed to advancing healthcare through innovation, quality, and compliance. At Sun Pharma, we empower professionals to grow, take ownership of their careers, and succeed in a collaborative and performance-driven environment.
Job Overview
Sun Pharma is seeking a detail-oriented Clinical Trial Assistant (CTA) to support clinical research operations through effective documentation management, regulatory support, and site coordination. This entry-level to early-career role is ideal for candidates looking to build a strong foundation in clinical research, GCP compliance, and trial administration within a global pharmaceutical environment.
Key Responsibilities
Documentation & Administrative Support
Assist in maintaining clinical study documentation, including protocols, informed consent forms (ICFs), case report forms (CRFs), and study reports
Organize and manage electronic and paper-based Trial Master Files (TMF), ensuring data accuracy and completeness
Provide administrative support by scheduling meetings, preparing agendas and minutes, and coordinating internal and external communications
Support travel coordination and logistics related to clinical trial activities
Regulatory & GCP Compliance Support
Assist in the preparation and submission of documents to Ethics Committees (ECs) and regulatory authorities
Support compliance with Good Clinical Practice (GCP) guidelines, SOPs, and applicable local regulations
Maintain regulatory trackers and essential document logs
Site Coordination & Vendor Management
Support tracking of site invoices, payment processes, and financial documentation
Assist with vendor code generation and vendor tracking activities
Coordinate with clinical sites, vendors, and internal stakeholders to ensure smooth trial operations
Educational Qualifications
Bachelor’s or Master’s degree in a health-related discipline such as Biology, Chemistry, Pharmacy, Nursing, Public Health, or Life Sciences
OR
Postgraduate Diploma in Clinical Research
Experience Required
0 to 2 years of relevant experience in Clinical Research or Clinical Trial Operations
Freshers with strong academic exposure and clinical research training may also be considered
Key Skills & Competencies
Basic understanding of clinical trial processes and GCP guidelines
Strong organizational and documentation skills
Good written and verbal communication abilities
Ability to manage multiple tasks in a structured and deadline-driven environment
Proficiency in MS Office and clinical documentation systems
Why Join Sun Pharma
At Sun Pharma, your professional development and well-being are a priority. We offer exposure to global clinical research programs, structured learning opportunities, and a collaborative workplace where your contributions make a real impact on patient outcomes worldwide.
Disclaimer
The above 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 or qualifications. Sun Pharma Laboratories Ltd reserves the right to modify responsibilities or assign additional duties based on organizational needs and candidate capabilities.
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