TCS is hiring for Clinical Operations/ETMF professionals to support clinical research and trial management. If you have experience in clinical operations and a background in life sciences, this could be your next career opportunity!
Key Responsibilities:
- Organize study start-up teleconferences with study teams.
- Assist in study start-up activities, ensuring compliance with Drug Shipment SOPs.
- Maintain accurate data entry in clinical study systems with high integrity.
- Support Clinical Study Teams in meeting urgent deliverables and maintaining inspection readiness.
- Assist in study close-out activities, ensuring compliance with SOPs and effective study closure.
- Compile and generate Clinical Study Report (CSR) Modular Appendices.
- Manage and archive essential documents per Sponsor TMF SOPs.
- Ensure adherence to process KPIs for assigned studies.
- Participate in meetings with Client and TCS teams.
Required Skills & Qualifications:
- Educational Qualification: Any Life Science Graduate (B.Sc./M.Sc./B.Pharm/M.Pharm/ Pharm.D).
- Experience: 2-9 years in Clinical Research, Clinical Operations, or ETMF (Electronic Trial Master File).
- Preferred Skills:
- Knowledge of clinical trial documentation and regulatory compliance.
- Familiarity with TMF (Trial Master File) management.
- Strong organizational and data management skills.
About Tata Consultancy Services (TCS)
TCS is a global leader in IT services, consulting, and business solutions, with a strong presence in the pharmaceutical and healthcare sectors. Known for innovation and excellence, TCS offers a dynamic work environment with opportunities for career growth and skill development.
How to Apply?
Interested candidates can share their resumes with:
📧 Email: babeeta.shahi@tcs.com
Why Apply?
✅ Reputed MNC with global recognition
✅ On-site job opportunity in Mumbai, Pune, or Bangalore
✅ Competitive salary & benefits
✅ Growth in clinical research & operations
