Tata Consultancy Services (TCS), a global leader in IT services and consulting, is hiring for multiple roles in the Life Sciences domain across Pune and Bengaluru. If you are a pharmacovigilance professional, clinical data expert, SAS programmer, or medical reviewer, this is your chance to join one of India’s most prestigious companies.
🚀 Open Positions & Eligibility Criteria
📍 TCS Pune – Walk-in on 13th April 2025
Location: Sahyadri Park, Rajiv Gandhi Infotech Park, Hinjewadi Phase 3, Pune
Walk-in Date & Time: Sunday, 13th April 2025 (10:00 AM – 03:00 PM)
Contact Person: Divya Amin
1. Submission Specialist (Job ID: 356642)
- Experience Required: 1-3 years
- Qualifications: B.Pharm/M.Pharm
- Key Skills: Experience in ICSR submissions using Argus
2. Medical Reviewer (Job ID: 356354)
- Experience Required: 1-4 years
- Qualifications: MBBS/MD only
- Key Skills: Reviewing adverse event reports, assessing drug safety
📍 TCS Bengaluru – Walk-in on 12th April 2025
Location: Think Campus, Electronic City Phase 2, Bengaluru
Walk-in Date & Time: Saturday, 12th April 2025 (10:00 AM – 02:00 PM)
Contact Person: Vidyalakshmi Rawat
1. Medical Reviewer (Job ID: 356306)
- Experience Required: 1-4 years
- Qualifications: MBBS/MD only
- Key Skills: Pharmacovigilance, adverse event assessment
2. Clinical Data Reviewer (Job ID: 15670M)
- Experience Required: 1-4 years
- Key Skills: Data discrepancy management, protocol compliance
3. SAS Programmer (Job ID: 356822)
- Experience Required: 2-8 years
- Key Skills: SAS programming (SDTM, ADAM, TFL)
4. Study Delivery Specialist (Job ID: 356261)
- Experience Required: 1-4 years
- Key Skills: Clinical research associate (CRA) experience
5. Project Pipeline Manager (Job ID: 356344)
- Experience Required: 5-10 years
- Key Skills: Clinical trial project management (Planisware/MS Project preferred)
6. Study Data Manager (Job ID: 356207)
- Experience Required: 5+ years
- Key Skills: End-to-end clinical data management
📌 Job Responsibilities
For Medical Reviewers (Pune & Bengaluru)
- Analyze patient adverse event reports in pharmacovigilance databases.
- Evaluate drug safety signals and potential risks.
- Provide medical expertise for case assessments.
For Submission Specialists (Pune)
- Handle ICSR (Individual Case Safety Report) submissions in Argus.
- Ensure compliance with global pharmacovigilance regulations.
For SAS Programmers (Bengaluru)
- Develop SDTM, ADAM, and TFL datasets for clinical trials.
- Perform statistical analysis using SAS.
- Ensure adherence to CDISC standards.
For Clinical Data Reviewers (Bengaluru)
- Conduct data discrepancy management as per study protocols.
- Perform external vendor data reconciliation.
For Study Delivery Specialists (Bengaluru)
- Manage clinical trial monitoring (CRA activities).
- Oversee site management and patient recruitment.
For Project Pipeline Managers (Bengaluru)
- Lead clinical trial project planning and execution.
- Use Planisware/MS Project for tracking progress.
For Study Data Managers (Bengaluru)
- Oversee end-to-end clinical data management.
- Ensure data integrity and quality control.
🏢 About TCS (Tata Consultancy Services)
TCS is a global IT powerhouse and part of the Tata Group, with a strong presence in life sciences, healthcare, and clinical research. Known for its employee-friendly policies, career growth opportunities, and competitive salaries, TCS is a preferred employer for professionals in the pharma and healthcare sectors.
📝 How to Apply?
Walk-in Interview Details
✅ Documents to Carry:
- Updated resume + TCS application form
- Original & photocopy of ID proof (Aadhar, PAN, Passport, Voter ID)
- Degree certificates + Marksheets (SSC, HSC, all semesters)
- 1 passport-size photograph
