Job Overview
| Particulars | Details |
|---|---|
| Position | Pharmacovigilance & Clinical Data Management |
| Company | Tata Consultancy Services |
| Location | Pune |
| Job Type | Full-Time |
| Experience | Fresher |
| Category / Department | Data Scientist |
| Application Mode |
🏢 About Tata Consultancy Services
Tata Consultancy Services (TCS) is a global technology and business solutions organization that works with clients across industries and geographies. Its broad capabilities include technology services, consulting, digital transformation, and solutions supporting sectors such as healthcare and life sciences.
Company Mission
TCS focuses on helping organizations transform and grow through technology, innovation, and business expertise while creating long-term value for its customers and stakeholders.
Company Vision
The organization aims to help businesses navigate evolving technology landscapes and create sustainable growth through innovation, digital capabilities, and collaborative solutions.
Core Values
🔹 Integrity and ethical conduct
🔹 Customer focus
🔹 Excellence and quality
🔹 Innovation and continuous learning
🔹 Collaboration and teamwork
🔹 Respect for people and communities
What Makes Them Different
TCS combines technology expertise with industry knowledge to deliver solutions for complex business challenges. Its work across healthcare and life sciences provides professionals with opportunities to contribute to global projects involving pharmaceutical operations, clinical research, data, and technology.
Leadership / Company Philosophy
TCS emphasizes continuous learning, professional development, collaboration, and long-term career growth. The organization encourages employees to develop expertise across evolving technologies and industry domains while contributing to meaningful client outcomes.
📍 Tata Consultancy Services Ltd.
A1 Interview Area
Sahyadri Park
💡 Editor's Note / Preparation Tip
📄 Resume Preparation Tips
1️⃣ Clearly specify whether your expertise is in Pharmacovigilance or Clinical Data Management.
2️⃣ Mention your exact years of relevant experience and key responsibilities handled.
3️⃣ For PV roles, highlight experience in case processing, adverse events, literature surveillance, and safety data review.
4️⃣ For CDM roles, highlight experience in data review, query management, data cleaning, database validation, and database lock.
5️⃣ Include relevant knowledge of GCP, CDISC, SOPs, regulatory requirements, and quality processes.
🎯 Interview Preparation
1️⃣ Revise key Pharmacovigilance concepts such as adverse events, serious adverse events, case processing, safety data, and literature surveillance.
2️⃣ For CDM interviews, prepare topics related to clinical data review, queries, data cleaning, validation, and database lock.
3️⃣ Review the fundamentals of GCP, CDISC standards, SOPs, and regulatory compliance.
4️⃣ Prepare examples from your previous projects that demonstrate your attention to detail and ability to meet quality and timeline requirements.
5️⃣ Be ready to explain how you identify discrepancies, manage queries, and ensure data or documentation quality.
💡 Professional Tips
1️⃣ Understand the complete clinical trial lifecycle and where Pharmacovigilance and CDM functions fit into the process.
2️⃣ Strengthen your knowledge of global drug safety regulations and clinical research standards.
3️⃣ Develop strong documentation and communication skills, as both roles require extensive collaboration and accurate records.
4️⃣ Be prepared to discuss the tools, databases, or systems you have used in your previous projects.
5️⃣ Carry all required documents in an organized folder and arrive early for the walk-in interview.
📝 Job Description
🚨 Walk-In Interview | Pharmacovigilance & Clinical Data Management | Tata Consultancy Services (TCS)
🌟 TCS is Hiring Experienced Professionals in Pune!
Looking to advance your career in Pharmacovigilance, Drug Safety, or Clinical Data Management? Tata Consultancy Services (TCS) is conducting a Walk-In Recruitment Drive in Pune for experienced professionals across Pharmacovigilance and Clinical Data Management (CDM).
Candidates with relevant experience in pharmaceutical, healthcare, clinical research, or life sciences domains can attend the walk-in interview on 26 July 2026 (Sunday). This is an excellent opportunity to work with a global technology and life sciences leader while gaining exposure to international projects and expanding your professional expertise. 💊🧪📊
Position Details
Company: Tata Consultancy Services (TCS)
Job Roles: Pharmacovigilance / Clinical Data Management
Job Type: Full-Time
Work Mode: Not Specified
Location: Pune, Maharashtra
Experience:
• Pharmacovigilance: 1–5 Years
• Clinical Data Management: 2–6 Years
Qualification: B.Pharm, M.Pharm, Pharm.D, B.Sc, M.Sc, Life Sciences, Biotechnology, Nursing, Allied Health Sciences, or relevant healthcare/life sciences qualifications
Interview Mode: Walk-In Interview
Walk-In Date: 26 July 2026 (Sunday)
Reporting Time: 10:00 AM – 02:00 PM
Preferred Skills
⭐ Experience in global Pharmacovigilance or Drug Safety operations
⭐ Knowledge of adverse event and safety case processing
⭐ Experience with literature monitoring and surveillance
⭐ Understanding of global regulatory requirements
⭐ Hands-on experience in clinical data review and query management
⭐ Knowledge of clinical database cleaning and validation
⭐ Familiarity with CDISC, GCP, and SOP compliance
⭐ Experience supporting clinical trial database lock activities
⭐ Strong documentation and quality management skills
Candidate Requirements
🎓 Candidates with relevant full-time qualifications may include:
• B.Pharm
• M.Pharm
• Pharm.D
• B.Sc
• M.Sc
• Life Sciences
• Biotechnology
• Nursing
• Allied Health Sciences
• Other relevant healthcare or life sciences qualifications
💼 Pharmacovigilance: 1–5 years of relevant experience
💼 Clinical Data Management: 2–6 years of relevant experience
🧪 Relevant experience in Pharmacovigilance, Drug Safety, Clinical Data Management, or related clinical research functions
📚 Strong understanding of applicable industry processes and quality requirements
🤝 Good communication, documentation, and collaboration skills
Why Join Tata Consultancy Services (TCS)?
🌍 Work with a globally recognized technology and business solutions organization
💊 Build a career in Pharmacovigilance and Clinical Data Management
🧪 Gain exposure to international pharmaceutical and healthcare projects
📈 Explore long-term career growth opportunities
📚 Access learning, upskilling, and professional certification opportunities
💼 Benefit from a structured professional work environment
🏆 Work with multidisciplinary teams across technology, healthcare, and life sciences
🌐 Gain valuable experience working on global client engagements
How to Apply
🚨 Walk-In Interview Opportunity
📅 Date: 26 July 2026 (Sunday)
⏰ Reporting Time: 10:00 AM – 02:00 PM
📍 Venue: Tata Consultancy Services Ltd., A1 Interview Area, Sahyadri Park 1, Hinjewadi Phase 3, Pune, Maharashtra
📌 Important: Carry both originals and photocopies of all required documents.
⚠️ Recruitment Safety Notice: TCS does not charge any fee at any stage of the recruitment process. Candidates are advised to participate only through official recruitment channels.
Know someone who would be a great fit? Tag them or share this opportunity with your network! 🚀
🎯 Key Responsibilities
- ✓ 1️⃣ Pharmacovigilance / Drug Safety
- ✓ Perform case processing and safety data review activities.
- ✓ Support documentation and assessment of adverse events and safety information.
- ✓ Conduct literature surveillance activities as required.
- ✓ Ensure pharmacovigilance activities align with applicable global regulatory guidelines.
- ✓ Perform quality reviews of safety-related documentation.
- ✓ Maintain accurate and complete safety records and documentation.
- ✓ Support compliance with established processes, procedures, and quality standards.
- ✓ Collaborate with relevant stakeholders to ensure timely completion of drug safety activities.
- ✓ 2️⃣ Clinical Data Management (CDM)
- ✓ Review and validate clinical trial data for completeness and accuracy.
- ✓ Generate, review, and resolve clinical data queries.
- ✓ Perform data cleaning activities throughout the clinical trial lifecycle.
- ✓ Conduct database quality checks and identify data inconsistencies.
- ✓ Ensure compliance with applicable CDISC standards, GCP requirements, and SOPs.
- ✓ Support clinical trial database lock activities.
- ✓ Contribute to maintaining high-quality clinical trial databases.
- ✓ Collaborate with clinical research and data management teams to address data-related issues.
💡 Required Qualifications & Skills
🚀 Career Guidance & Interview Insights
To help you succeed, we've compiled original preparation guides, resume keywords, and growth analytics for this category of role.
This Pharmacovigilance & Clinical Data Management role is a chance to contribute directly to life sciences, patient care, or pharmaceutical advancements. You will work within strict compliance frameworks, ensure rigorous quality standards, and collaborate with technical or medical experts. It is a career path that blends scientific excellence with a deep sense of social purpose.
Healthcare and pharmaceutical professionals grow through specialized scientific experience. Entry-level starts as Lab Technician, Chemist, or Quality Associate, progressing to Senior QA/QC Analyst. Advancement leads to Lab Supervisor, Clinical Project Manager, and senior management roles like Quality Director, VP of Regulatory Affairs, or Chief Scientific Officer.
Expected Technical & Behavioral Questions:
- Q1: How do you ensure compliance with WHO/GMP guidelines during laboratory operations?
Answer Tip: Mention strict adherence to Standard Operating Procedures (SOPs), detailed batch records, regular equipment calibration, and sanitization cycles. - Q2: What steps do you take when a quality deviation is detected in a product batch?
Answer Tip: Outline immediate isolation of the batch, raising a deviation report, root cause analysis (RCA), and initiating CAPA (Corrective and Preventive Action). - Q3: How do you manage safety protocols while handling toxic chemicals?
Answer Tip: Discuss using Material Safety Data Sheets (MSDS), wearing appropriate Personal Protective Equipment (PPE), proper ventilation, and chemical spill kits.
To pass automated ATS (Applicant Tracking System) screening and catch the recruiter's eye, tailor your resume with the following tips:
- Keywords to include: Quality Control (QC), GMP Compliance, FDA Regulations, SOP Documentation, HPLC/GC analysis, Batch Validation, Clinical Trials, Pharmacovigilance.
- Format: List laboratory skills and instruments handled (e.g. HPLC, spectrophotometer) in a dedicated technical matrix.
- Quantify Results: E.g., 'Validated 15 batch formulations under GMP guidelines with zero quality defects.'
Estimated compensation for this role type in India is ₹2,40,000 - ₹3,80,000 per annum (Fresher analyst). The actual salary package offered depends on factors such as company size, work mode (remote or on-site), individual technical proficiency, and negotiations during final HR rounds.
Key credentials: GMP Certified Professional (ASQ), Certified Clinical Research Coordinator (CCRC), or specialized laboratory training certificates in high-performance liquid chromatography (HPLC) and safety standards.
Frequently Asked Questions
1️⃣ Where is the TCS Walk-In Interview being conducted?
The walk-in interview will be conducted at Tata Consultancy Services Ltd., A1 Interview Area, Sahyadri Park 1, Hinjewadi Phase 3, Pune, Maharashtra.
2️⃣ What is the interview date and reporting time?
The interview is scheduled for 26 July 2026 (Sunday), with reporting between 10:00 AM and 02:00 PM.
3️⃣ How much experience is required?
For Pharmacovigilance, candidates with 1–5 years of relevant experience are eligible. For Clinical Data Management, candidates with 2–6 years of relevant experience are eligible.
4️⃣ What qualifications are accepted?
Relevant full-time qualifications may include B.Pharm, M.Pharm, Pharm.D, B.Sc, M.Sc, Life Sciences, Biotechnology, Nursing, Allied Health Sciences, and other relevant healthcare or life sciences degrees, subject to TCS hiring criteria.
5️⃣ What documents should candidates carry?
Candidates should carry both originals and photocopies of the required documents, including resume, photograph, PAN Card, Aadhaar Card, TCS Application Form, educational documents, mark sheets, degree/provisional certificate, salary proof, passport/passport application receipt, and updated EPFO Service History.
6️⃣ Does TCS charge any recruitment fee?
No. TCS does not charge any fee at any stage of the recruitment process. Candidates should participate only through official recruitment channels.
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