Healthcare Job at Sun Pharma: Apply Now For Executive Position
Healthcare Job: Sun Pharma is looking for a detail-oriented and motivated Executive – Trial Master File (eTMF) to support clinical research operations. This role is ideal for fresh graduates or early-career professionals who want to build expertise in documentation, compliance, and eTMF system management within a global pharmaceutical environment. If you’re someone who values quality, precision, and continuous learning, this opportunity offers a strong foundation to grow.
Healthcare Job – Details
- Position: Executive – Trial Master File (eTMF)
- Business Unit: Clinical Research
- Location: Sun House – Corporate Office, Mumbai
- Experience Required: 0–2 years
About the Company
Sun Pharma is the world’s fourth-largest specialty generic pharmaceutical company, known for its strong commitment to innovation, research excellence, and patient-centric healthcare solutions. With a presence in over 100 countries, Sun Pharma fosters a culture that encourages growth, leadership, and collaboration.
The organization thrives on its philosophy of “Create Your Own Sunshine”—empowering employees to take charge, evolve continuously, and succeed together in a supportive and progressive environment. At Sun Pharma, you don’t just build a career—you build a brighter future.
Healthcare Job – Qualifications
- Bachelor’s or master’s degree in a health-related field, such as Public Health
- OR a Post-Graduate Diploma in Clinical Research
- 0–2 years of relevant experience in clinical research or documentation
- Strong attention to detail and familiarity with documentation workflows preferred
About the Role
The Executive – eTMF plays a crucial role in managing and maintaining essential clinical trial documentation within the electronic Trial Master File system. This position ensures all records meet regulatory, quality, and compliance requirements. You will support study teams, collaborate with CRAs, maintain audit readiness, and enhance documentation processes. The role is ideal for individuals who enjoy organized systems, structured workflows, and contributing to the integrity of clinical research operations.
Key Responsibilities
Documentation & Administrative Support
- Organize, review, and maintain all trial-related documents with accuracy and completeness
- Perform quality checks and ensure regulatory compliance
- Maintain version control and follow document lifecycle standards
System Oversight
- Manage and update the eTMF system
- Maintain folder structures and ensure system functionality
- Ensure regular uploads and reconciliation of essential documents
Regulatory Compliance Support
- Keep the eTMF inspection-ready at all times
- Serve as the primary contact during audits for TMF-related queries
Process Improvement
- Evaluate and enhance eTMF workflows to improve efficiency
- Suggest improvements in documentation management processes
Coordination & Communication
- Coordinate with CRAs for timely TMF updates
- Conduct periodic TMF gap analyses and report insufficiencies
- Support cross-functional teams as needed
