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Clinical Data / Pharmacovigilance / Regulatory / Clinical Operations Associate

Tata Consultancy Services (Tcs)
TATA CONSULTANCY SERVICES (TCS)
0-1 years
₹3 LPA – ₹4.5 LPA
Navi Mumbai, India
10 March 13, 2026
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Clinical Data / Pharmacovigilance / Regulatory / Clinical Operations Associate

Company: Tata Consultancy Services (TCS)
Location: Navi Mumbai / Mumbai, India
Job Type: Full-Time
Experience: 0 – 6 Months (Freshers)
Qualification: B.Pharm
Eligible Batch: 2025 & 2026
Approx Salary: ₹3 LPA – ₹4.5 LPA


Job Overview

Tata Consultancy Services (TCS) is hiring B.Pharm freshers for roles in Clinical Data Management, Pharmacovigilance, Regulatory Affairs, and Clinical Operations. This opportunity is ideal for pharmacy graduates looking to start a career in clinical research, drug safety, regulatory compliance, and life sciences data management. Selected candidates will work on projects for global pharmaceutical and healthcare clients within TCS Life Sciences operations.


Key Responsibilities

1. Clinical Data Management

  • Process and validate clinical trial data to ensure accuracy and completeness.

  • Support Electronic Data Capture (EDC) systems used in clinical trials.

  • Ensure compliance with regulatory standards for clinical data management.

2. Pharmacovigilance

  • Review adverse event (AE) reports and assist in safety case processing.

  • Support pharmacovigilance database maintenance and safety documentation.

  • Assist in regulatory safety reporting and compliance activities.

3. Regulatory Affairs

  • Support preparation and review of regulatory documentation and submissions.

  • Assist with compliance activities related to global regulatory guidelines.

  • Maintain regulatory records and documentation for pharmaceutical projects.

4. Clinical Operations

  • Assist in managing clinical trial documentation and records.

  • Support coordination of clinical research activities.

  • Ensure adherence to clinical protocols and regulatory requirements.


Required Skills

Technical Skills

  • Basic knowledge of clinical research and drug development processes

  • Understanding of pharmacovigilance and regulatory guidelines

  • Clinical data management and documentation skills

  • Familiarity with clinical trial processes and compliance requirements

Soft Skills

  • Strong attention to detail

  • Analytical and problem-solving abilities

  • Effective communication and teamwork skills

  • Ability to work in rotational shifts and collaborative environments


Selection Process

  1. Aptitude Test

  2. Technical / HR Interview

Candidates must successfully clear each stage to proceed to the next step in the recruitment process.


Walk-in Interview Details

Interview Date: 23 March 2026
Time: 10:00 AM – 12:00 PM

Venue:
Anjuman-I-Islam’s Kalsekar Technical Campus
Plot No. 2 & 3, Sector-16
Near Thana Naka, Khanda Gaon
Panvel, Navi Mumbai, Maharashtra – 410206


Documents Required

  • Updated Resume

  • Government ID Proof (Aadhar / PAN)

  • Academic Documents (Original + Copies)

  • TCS Application Form

Note: Name, Date of Birth, and Address on the application form must match Aadhar card details.


Role Impact

This role provides pharmacy graduates with the opportunity to gain hands-on experience in clinical research, pharmacovigilance, regulatory compliance, and life sciences data management, while working with global pharmaceutical clients through TCS’s life sciences operations.