TCS Walk-In Drive 2026 for Pharmacovigilance & Clinical Data Management Jobs in Pune

Pharmacovigilance and Clinical Data Management continue to be among the fastest-growing career domains in the pharmaceutical and clinical research industry. As global pharmaceutical companies focus on developing safer medicines and conducting high-quality clinical trials, the demand for professionals skilled in drug safety, adverse event reporting, clinical trial data review, and regulatory compliance has increased significantly. For experienced candidates looking to advance their careers, opportunities with globally recognized organizations provide valuable exposure to international healthcare projects and long-term professional growth.

Tata Consultancy Services (TCS), one of India’s largest technology and life sciences service providers, has announced a Walk-In Recruitment Drive for experienced professionals in Pharmacovigilance and Clinical Data Management (CDM). The walk-in interview will be conducted at the company’s Pune office, offering eligible candidates the chance to join a globally respected organization that delivers healthcare, pharmaceutical, and life sciences solutions to leading clients worldwide.

Whether you are currently working in Drug Safety Operations, Individual Case Safety Report (ICSR) processing, Clinical Data Management, or clinical trial database activities, this recruitment drive provides an excellent opportunity to take the next step in your professional journey while working on global pharmaceutical projects.

📋 Walk-In Drive Overview

🏢 About Tata Consultancy Services (TCS)

Tata Consultancy Services (TCS) is one of the world’s leading IT services, consulting, and business solutions organizations. Apart from technology services, TCS has built a strong presence in the Life Sciences and Healthcare sector by supporting pharmaceutical companies, biotechnology organizations, medical device manufacturers, and Contract Research Organizations (CROs) across the globe.

The company works on a wide range of healthcare projects including Pharmacovigilance, Clinical Data Management, Regulatory Affairs, Medical Writing, Clinical Operations, Real World Evidence, and Healthcare Analytics. Employees get the opportunity to collaborate with global clients while working in a structured environment focused on learning, innovation, and career development.

💼 Available Job Roles

1️⃣ Pharmacovigilance

Candidates with experience in Pharmacovigilance or Drug Safety Operations can participate in the walk-in drive. This role focuses on monitoring the safety of pharmaceutical products, reviewing adverse events, maintaining regulatory compliance, and ensuring patient safety throughout the product lifecycle.

Professionals working in Pharmacovigilance contribute significantly to global healthcare by evaluating medicine safety data and supporting timely regulatory reporting.

2️⃣ Clinical Data Management (CDM)

The Clinical Data Management profile is suitable for professionals involved in clinical trial data review, database validation, query management, data cleaning, and database lock activities. Clinical Data Management ensures that clinical trial information is accurate, complete, and compliant with international regulatory requirements before study completion.

This role offers exposure to global clinical trials, Electronic Data Capture (EDC) systems, and international data quality standards used by leading pharmaceutical companies.

📌 Key Responsibilities

Depending on the role selected during the recruitment process, candidates may perform the following responsibilities:

Pharmacovigilance Responsibilities

• Review and process Individual Case Safety Reports (ICSRs).
• Perform adverse event and serious adverse event documentation.
• Support literature surveillance and case assessment activities.
• Ensure compliance with global pharmacovigilance regulations and SOPs.
• Maintain high standards of quality and documentation accuracy.
• Participate in quality review and regulatory reporting activities.

Clinical Data Management Responsibilities

• Review and validate clinical trial data.
• Generate and resolve data queries.
• Perform database cleaning and quality review.
• Support database lock activities.
• Maintain compliance with GCP, CDISC standards, and company SOPs.
• Coordinate with project teams to ensure timely completion of data management milestones.

🎓 Eligibility Criteria

TCS is looking for professionals who already have hands-on experience in Pharmacovigilance or Clinical Data Management. Candidates should ensure that they meet the required experience before attending the walk-in interview. Those with relevant domain expertise and a strong understanding of healthcare processes will have an advantage during the selection process.

Pharmacovigilance

• 1 to 5 years of relevant Pharmacovigilance or Drug Safety experience.
• Knowledge of adverse event processing and safety documentation.
• Understanding of global pharmacovigilance regulations and quality standards.

Clinical Data Management (CDM)

• 2 to 6 years of Clinical Data Management experience.
• Experience in clinical trial data review and validation.
• Knowledge of query management, database cleaning, and database lock activities.
• Familiarity with GCP, CDISC guidelines, and clinical research SOPs will be beneficial.

🎓 Educational Qualification

Candidates with full-time qualifications in healthcare, pharmacy, or life sciences are generally eligible, subject to TCS hiring guidelines.

• B.Pharm
• M.Pharm
• Pharm.D
• B.Sc
• M.Sc
• Life Sciences
• Biotechnology
• Nursing
• Allied Health Sciences
• Other relevant healthcare or life sciences qualifications

📄 Documents Required

Candidates should carry both original documents and self-attested photocopies for verification during the interview process.

• Updated Resume/CV.
• Recent Passport-size Photograph.
• PAN Card.
• Aadhaar Card.
• TCS Application Form (if applicable).
• Highest Educational Qualification Certificates.
• All Semester Mark Sheets.
• Consolidated Mark Sheet.
• Degree or Provisional Certificate.
• Latest Salary Revision/Hike Letter.
• Valid Passport or Passport Application Receipt.
• Updated EPFO Service History.

📍 Walk-In Interview Details

🌟 Why Join TCS?

Joining Tata Consultancy Services offers more than just a job. It provides an opportunity to work with one of the world’s most respected organizations while contributing to international pharmaceutical and healthcare projects. Employees receive exposure to modern technologies, structured training programs, and opportunities to collaborate with global clients.

• Work with a globally recognized IT and Life Sciences company.
• Exposure to international pharmaceutical projects.
• Excellent learning and certification opportunities.
• Professional and collaborative work culture.
• Competitive salary and employee benefits.
• Long-term career growth within healthcare and life sciences.

💡 Interview Preparation Tips

Since this walk-in drive is intended for experienced professionals, candidates should be prepared to discuss their previous projects, daily responsibilities, and domain knowledge during the interview.

• Revise your previous project experience.
• Be ready to explain your role and responsibilities.
• Understand current Pharmacovigilance or CDM workflows.
• Carry a well-formatted and updated resume.
• Reach the venue before the reporting time to avoid delays.

📈 Career Growth

Professionals joining TCS in Pharmacovigilance or Clinical Data Management can build rewarding careers across multiple healthcare domains. With experience, employees may progress into senior specialist, team lead, project management, quality assurance, regulatory compliance, or global clinical operations roles. The exposure gained through international projects also enhances future career opportunities within pharmaceutical companies, CROs, and healthcare organizations worldwide.

⚠️ Important Note

📝 Final Thoughts

The TCS Walk-In Recruitment Drive in Pune presents an excellent opportunity for experienced Pharmacovigilance and Clinical Data Management professionals seeking career advancement with a globally recognized organization. If you meet the eligibility criteria, prepare your documents carefully, update your resume, and attend the walk-in interview on the scheduled date. Working with TCS can provide valuable international exposure, continuous learning opportunities, and a strong platform for long-term growth in the pharmaceutical and clinical research industry.