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TCS is hiring for Pharmacovigilance, Medical Reviewer
PV - Case Processing
Eligibility Criteria : Pharmacovigilance : B.Pharm / M.Pharm graduate with experience in drug safety, case processing, ICSR, ARGUS or ARISG.
Location : Mumbai, Pune
Responsibilities :
1. Ability to understand and analyses the complex data and performs the activities including accessing the case in Argus, code and enter data.
2. Be fully competent to perform all steps within the case-handling process.
3. Ensure compliance with global and local procedural documents and local implementation of Patient Safety objectives, policies, processes and procedures.
4. Responsible for follow up procedures.
5. Contribute to the development and implementation of new safety-related systems, processes and procedures within the process.
6. Support a performance-driven culture.
7. Excellent communication skills (verbal and written)
8. Ability to work in team and meet the strict timelines of delivery
Medical Reviewer
Eligibility Criteria : MBBS/MD Professional only. A medical reviewer in pharmacovigilance reviews patient adverse events in a database to assess drug safety and potential risks.
Location : Mumbai
Responsibilities :
• Accountable for the medical review of relevant clinical, other solicited and spontaneous cases (including literature articles), medical assessment (including labeling and causality along with the company causality statement)
• Review the medical sense including seriousness and coding of the case in the global context of the drug or clinical project, including the narrative, AE/SAE terms, suspect drugs, concomitant medications, laboratory data, and medical history
• Developing and maintaining thorough knowledge of the appropriate disease biology areas & important safety concerns for marketed drugs and drugs in development
• Assuring and maintaining compliance with regulatory and local/global SOP timelines TCS Confidential
• Supporting the Drug Safety teams with medical concepts and awareness of product related topics to ensure quality of adverse event data processing
• Representing safety physician team in internal and client safety forums and audits
• Review and respond to any queries/comments for an individual case safety report in the Patient Safety database.
• Responsible for generating, sending, and tracking medically relevant queries for follow-up information that is required for an individual case safety report
• Provide product advice as required, especially with regards to case reports that are Suspected Unexpected Serious Adverse reaction (SUSAR)
• Ensure compliance with global and local procedural documents and implementation of client and TCS, policies, procedures, and processes.
Walk in Interview
Saturday, 05th July 2025, 10:00 AM - 12:30 PM
Tata Consultancy Services Ltd, Wellspring, Plant No 12, Gate No 4 Godrej & Boyce complex LBS Marg, Vikhroli Mumbai - 400079
Apply Online
Pharmacovigilance : Click here
Medical Reviewer : Click here
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