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Build Your Future with a Tata Consultancy Services Job – Apply Today!

Build Your Future with a Tata Consultancy Services Job – Apply Today!

If you are looking for a rewarding Tata Consultancy Services job, this Medical Specialist opening offers an excellent opportunity to grow your career in the life sciences domain. As one of the most trusted companies in India, Tata Consultancy Services provides a stable and growth-oriented environment, making it a great choice for professionals exploring Tata Consultancy Services careers in medical review, clinical safety, and regulatory compliance.

Job Details: 

  • Job Position: Medical Specialist (Medical Reviewer)

Qualifications:

• Minimum qualification: MBBS or equivalent
• Strong understanding of pharmacovigilance and clinical data review
• Knowledge of therapeutic areas and drug-safety processes
• Excellent analytical, communication, and documentation skills

About the Company:

Tata Consultancy Services is a global leader in IT services, consulting, and business solutions. Known for its innovation-driven culture, TCS supports clients worldwide across industries, including banking, healthcare, and life sciences. For professionals seeking long-term growth, Tata Consultancy Services careers offer continuous learning and opportunities to work on impactful global projects.

Tata Consultancy Services Job Description:

This job involves comprehensive medical review responsibilities in the life sciences domain. The Medical Specialist will handle clinical case assessments, evaluate data from solicited and spontaneous reports, and review literature-based cases. You will examine adverse events, narratives, and medical histories while ensuring compliance with global safety standards. This role is ideal for professionals aspiring to expand their expertise through Tata Consultancy Services careers focused on medical evaluation and regulatory compliance.

Tata Consultancy Services job – Key Responsibilities:

• Perform medical review of clinical, solicited, and spontaneous cases
• Assess labeling, causality, and prepare company causality statements
• Review the seriousness and coding of cases in a global drug-safety context
• Evaluate AE/SAE terms, suspect medications, lab results, and patient histories
• Maintain updated knowledge of disease biology and key safety concerns
• Ensure adherence to global and local SOP timelines and regulatory guidelines

LINK FOR THE ORIGINAL NOTIFICATION

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