Sun Pharma Public Health Job Opportunity – eTMF Executive Role
Sun Pharma Laboratories Ltd has announced a fresher’s public health job opportunity for the position of eTMF Executive within its Clinical Research division in Mumbai. This opening under Sun Pharma careers is ideal for candidates seeking entry-level exposure to clinical research, documentation management, and regulatory compliance while working with one of India’s leading pharmaceutical organizations.
Job Details:
- Job Position: Executive – Trial Master File (eTMF Executive)
- Company Name: Sun Pharma Laboratories Ltd
- Job Location: Mumbai (Sun House – Corporate Office)
About the Company:
Sun Pharma Laboratories Ltd is one of India’s largest pharmaceutical companies and a trusted name in global healthcare. Known for its employee-focused culture, Sun Pharma careers emphasize continuous growth, accountability, and collaboration. Professionals exploring Sun Pharma jobs benefit from a supportive environment that encourages innovation and long-term career development in healthcare and public health job roles.
Qualifications:
Educational Qualification
The minimum qualification requirement is a Bachelor’s or Master’s degree in a health-related field, such as public health.
Experience
Relevant experience of 0–2 years minimum in the field of clinical research.
Public Health Job Description:
At Sun Pharma, we commit to helping you “Create your own sunshine”— by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community.
As you enter the Sun Pharma world, you’ll find yourself becoming ‘Better every day’ through continuous progress. Exhibit self-drive as you ‘Take charge’ and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we ‘Thrive together’ and support each other’s journeys. This public health job supports clinical research operations through effective trial documentation management.
Public Health Job – Key Responsibilities:
Documentation and Administrative Support
- Ensuring all trial-related documents are organized, accurate, and complete
- Reviewing and approving documents for quality and compliance
- Maintaining version control for all documents
System Oversight
- Maintaining the eTMF system, ensuring it’s up-to-date and functioning correctly
- Establishing and maintaining the eTMF’s structure and folder system
Regulatory Compliance Support
- Ensuring the eTMF system is inspection-ready for health authorities
- Serving as the point of contact for auditors during inspections for TMF related queries
Process Improvement
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Continuously evaluating and improving the eTMF processes and workflows to increase efficiency and compliance
Coordination & Communication
- Coordination and follow-up with CRAs to update TMF
- Perform periodic TMF gap analysis and communicate the insufficiency to CRAs
