Tata Consultancy Services (TCS), one of India’s leading global IT and life sciences service providers, is inviting applications from experienced Life Sciences professionals for two specialized roles in Regulatory Documents Processing and Clinical Trial Disclosures. These opportunities are ideal for candidates with strong experience in regulatory publishing, CT.gov submissions, and clinical trial transparency activities.
Both positions are work-from-office roles based in Mumbai, Pune, and Noida, offering stable career growth within TCS’s global life sciences delivery ecosystem.
Open Positions at TCS
1) Documents Processing – Regulatory Publishing
Key Responsibilities:
- Format and publish regulatory documents as per global health authority standards
- Ensure compliance with ICH, eCTD, and sponsor-specific formatting requirements
- Perform quality checks on regulatory submissions and life sciences documentation
- Collaborate with cross-functional regulatory and publishing teams
Shift & Work Model:
- Shift Timings: 3:00 PM – 11:00 PM
- Work Mode: 5 days Work From Office (WFO)
2) Clinical Trial Disclosures Specialist
Key Responsibilities:
- Perform ClinicalTrials.gov (CT.gov) registration and results posting
- Prepare and submit results summaries in compliance with global disclosure regulations
- Ensure timelines and regulatory compliance for clinical trial transparency
- Maintain documentation and audit readiness for disclosures
Shift & Work Model:
- Shift Timings: 10:00 AM – 8:00 PM
- Work Mode: 5 days Work From Office (WFO)
Qualifications & Experience (For Both Roles)
- Educational Qualification: Life Sciences Graduate (B.Pharm, M.Pharm, MSc, or related discipline)
- Experience: Minimum 4+ years of relevant hands-on experience
- Strong understanding of regulatory and clinical trial documentation standards
- Prior experience in pharma, CROs, or life sciences services is highly preferred
Job Locations
- Mumbai
- Pune
- Noida
Salary & Benefits
- Salary Range: ₹6,00,000 – ₹10,00,000 per annum (INR), depending on experience and skill set
- Structured career growth at TCS Life Sciences
- Exposure to global regulatory and clinical trial projects
- Stable work environment with long-term career prospects
How to Apply
Interested and eligible candidates can share their updated resume via email:
Tip: Mention the job title (Documents Processing or Clinical Trial Disclosures) clearly in the subject line for faster screening.
