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Tata Consultancy Services (TCS) has announced a major Walk-In Drive in Chennai on 29 November 2025 for experienced Life Sciences, Pharmacovigilance, Clinical Research, and SAS Programming professionals. Candidates with 1–15 years of experience can apply for high-demand roles including Medical Reviewer, Pharmacovigilance Case Processor, Clinical Safety Scientist, and Statistical Programmer.
This hiring initiative offers excellent opportunities for skilled healthcare and pharma professionals to join one of India’s most trusted employers. Below is the complete job guide to help candidates prepare effectively.
🔍 Available Positions & Job IDs
| Role | Job ID |
|---|---|
| Medical Reviewer | 382468 |
| Pharmacovigilance – Case Processing | 382636 |
| Clinical Safety Scientist | 382793 |
| Statistical Programmer (SAS) | 382120 |
📍 Walk-In Details
- Date: Saturday, 29 November 2025
- Time: 10:00 AM – 2:00 PM
- Venue:
Tata Consultancy Services Limited,
Siruseri SEZ Unit, Plot No.1/G1, SIPCOT I.T. Park,
Siruseri, Navalur Post, Kancheepuram District, Chennai – 603103 - Contact Persons: Vidyalakshmi Rawat / Manisha Singh
- Eligibility: Freshers Not Eligible
🧑🎓 Education Requirement
- Minimum 15 years of regular, full-time education (10 + 2 + 3)
🧪 Role-wise Responsibilities & Skills
1. Medical Reviewer (MBBS/MD)
Responsibilities
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- Perform medical review of PV cases
- Apply clinical judgment for safety assessment
- Ensure compliance with regulatory standards
Skills
- Strong understanding of pharmacovigilance terminology
- Medical review experience in global safety databases
2. Pharmacovigilance – Case Processing
Responsibilities
- Access, review, and process safety cases in Argus
- Code, assess, and enter data accurately
- Analyze complex clinical and safety data
Skills
- Hands-on experience in ICSR case processing
- Strong analytical and medical coding skills
3. Clinical Safety Scientist (MPharm/PhD/BDS)
Responsibilities
- Author & review PBRER, DSUR, RMP
- Perform signal detection & signal management
- Collaborate with global safety teams
Skills
- Regulatory writing expertise
- Good understanding of global safety regulations
4. Statistical Programmer – Clinical SAS
Responsibilities
- Create ADaM, TFL, SDTM datasets
- Support regulatory e-submission
- Work on integrated analysis for oncology/neuroscience/immunology studies
Skills
- Strong SAS programming
- Exposure to global clinical trial datasets
📄 Documents to Carry
- Aadhar + PAN (ID proof)
- 1 passport-size photo
- Updated resume (hard copy)
💼 Benefits of Working at TCS
- Stable long-term career growth
- Global regulatory & pharmacovigilance exposure
- Work-life balance & employee-friendly environment
- Opportunity to work on global clinical programs
📝 How to Apply
📍 Walk-In Details
- Date: Saturday, 29 November 2025
- Time: 10:00 AM – 2:00 PM
- Venue:
Tata Consultancy Services Limited,
Siruseri SEZ Unit, Plot No.1/G1, SIPCOT I.T. Park,
Siruseri, Navalur Post, Kancheepuram District, Chennai – 603103 - Contact Persons: Vidyalakshmi Rawat / Manisha Singh
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