Job Title: Clinical Trial Assistant
Company: Sun Pharma Laboratories Ltd
Business Unit: Clinical Research
Location: Mumbai, India (Sun House – Corporate Office)
Date Posted: February 4, 2026
Employment Type: Full-Time
Sun Pharma is a global specialty generic pharmaceutical company committed to innovation, quality, and patient-centric research. The organization fosters a growth-oriented, collaborative, and performance-driven culture, enabling professionals to build impactful and rewarding careers in clinical research and drug development.
Sun Pharma is seeking a Clinical Trial Assistant (CTA) to support clinical research activities through effective documentation, regulatory coordination, and site-level operational support. This role is ideal for early-career professionals looking to build a strong foundation in clinical trials, regulatory compliance, and study coordination within a global pharmaceutical environment.
The Clinical Trial Assistant will work closely with clinical research teams to ensure smooth execution of clinical studies in compliance with Good Clinical Practice (GCP), internal SOPs, and regulatory requirements.
Assist in the preparation, maintenance, and archival of clinical trial documentation, including protocols, informed consent forms (ICFs), case report forms (CRFs), and study reports.
Organize and maintain electronic and paper-based Trial Master Files (TMF), ensuring accuracy, completeness, and audit readiness.
Provide administrative support such as scheduling meetings, preparing agendas and minutes, and coordinating internal and external communications.
Support the preparation and submission of regulatory documents to Ethics Committees and regulatory authorities.
Assist in ensuring compliance with GCP guidelines, applicable regulatory requirements, and internal quality standards.
Support tracking of regulatory approvals, amendments, and essential documents throughout the study lifecycle.
Assist in tracking site invoices and supporting the invoice generation and payment process.
Support vendor code generation and maintain accurate vendor tracking records.
Coordinate with internal stakeholders, sites, and vendors to ensure timely execution of assigned tasks.
Bachelor’s or Master’s degree in a health-related discipline such as Life Sciences, Biology, Chemistry, Pharmacy, Nursing, or Public Health
OR
Postgraduate Diploma in Clinical Research
0 to 2 years of relevant experience in Clinical Research, Clinical Operations, or a related domain.
Freshers with strong academic credentials and formal training in clinical research may also be considered.
Basic understanding of clinical trial processes and GCP guidelines
Strong organizational and documentation skills
Attention to detail and ability to manage multiple tasks
Effective written and verbal communication skills
Proficiency in MS Office applications
Ability to work collaboratively in a team-oriented environment
Sun Pharma offers a supportive and inclusive work culture with opportunities for continuous learning, professional development, and career progression. Employees benefit from exposure to global clinical research projects and a strong commitment to personal growth and well-being.
This job description outlines the general nature and level of work expected for this role. Duties and responsibilities may evolve based on organizational needs and business requirements.
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