Pharmacovigilance Associate

Role Overview Tata Consultancy Services (TCS) is looking for a skilled Pharmacovigilance Associate to join its growing Healthcare & Life Sciences division in Hyderabad. This is a full-time, permanent opportunity suited for professionals with a strong background in drug safety operations, case processing, and regulatory compliance. You will be part of a high-performing team that plays a critical role in maintaining patient safety standards for global pharmaceutical clients. Key Responsibilities In this role, you will be responsible for reviewing and analysing complex adverse event data and processing individual case safety reports (ICSRs) using the Argus safety database. You will handle end-to-end case management, including data entry, medical coding, and quality review. Ensuring strict adherence to global and local regulatory guidelines, Patient Safety policies, and standard operating procedures will be a core part of your daily work. You will also be responsible for managing follow-up activities on pending safety cases and contributing to the continuous improvement of safety systems, processes, and workflows. Collaboration with cross-functional teams and meeting stringent submission timelines are essential expectations of this position. Required Qualifications Candidates must hold a Bachelor of Pharmacy (B.Pharma) degree or an equivalent qualification in life sciences. Prior hands-on experience in pharmacovigilance or drug safety, particularly with Argus safety software, is required. A solid understanding of healthcare domain practices and global pharmacovigilance regulations is expected. Why Join Us TCS is one of India's most respected IT and consulting organisations, offering a world-class work environment, structured career growth, and exposure to global pharmaceutical and life sciences clients. Working with TCS means being part of a performance-driven culture that values innovation, quality, and professional development at every level.

2 to 6 years of experience in pharmacovigilance or drug safety operations Hands-on expertise with Argus safety database for case access, data entry, and processing Proficiency in end-to-end individual case safety report (ICSR) handling Knowledge of global and local pharmacovigilance regulations and Patient Safety guidelines Experience with medical coding in the context of adverse event reporting Ability to manage follow-up procedures for open or incomplete safety cases Strong analytical skills for interpreting complex clinical and safety data Excellent verbal and written communication skills Ability to work collaboratively within a team and meet strict delivery timelines Bachelor of Pharmacy (B.Pharma) or equivalent degree in life sciences

Opportunity to work with a globally recognised IT and consulting leader Exposure to international pharmaceutical and life sciences clients Structured career development and learning programmes Performance-driven work culture with recognition initiatives Comprehensive employee support and wellness programmes