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

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