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Medical Reviewer Job for MBBS/MD Professionals at Tata Consultancy Services – Kickstart Your Career in Drug Safety!

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Explore a medical reviewer job at Tata Consultancy Services for MBBS and MD candidates. Apply now for top tata careers in drug safety and clinical research.
Medical Reviewer Job at TCS for MBBS & MD Graduates

Medical Reviewer Job at Tata Consultancy Services | Apply now

Looking for a medical reviewer job in a leading global company? Tata Consultancy Services (TCS) is offering an excellent opportunity for MBBS and MD professionals to build a career in pharmacovigilance and clinical research. This role is ideal for candidates interested in drug safety, regulatory processes, and advancing their careers through top tata careers opportunities.

Job Details

  • Job Position: Medical Reviewer
  • Location: India

About the Company

Tata Consultancy Services (TCS) is a globally recognized IT services, consulting, and business solutions organization. Known for innovation and excellence, TCS offers outstanding tata careers for healthcare professionals, including opportunities in pharmacovigilance, clinical research, and drug safety.

Job Description

This medical reviewer job involves reviewing clinical, solicited, and spontaneous cases, including literature reports, to ensure accurate drug safety evaluation and regulatory compliance. Responsibilities include medical assessment, causality determination, and case coding in a global context, along with analyzing AE/SAE terms, medications, lab data, and medical history. The role also requires maintaining knowledge of disease biology and safety concerns, ensuring compliance with SOP timelines, supporting drug safety teams, handling case queries and follow-ups, participating in audits, and providing guidance on serious adverse reactions like SUSARs.

Qualifications

  • MBBS or MD
  • Preferred experience: 9 months to 4 years
  • Experience in Pharmacovigilance or Clinical Research (drug safety) preferred

Key Responsibilities

  • Perform medical review and safety assessment of adverse event cases
  • Ensure accurate coding, labeling, and causality assessment
  • Maintain compliance with global pharmacovigilance regulations
  • Support drug safety teams with medical expertise
  • Handle case queries and follow-ups efficiently
  • Participate in audits and safety discussions

Skills Required

  • Computer Literate (e.g., knowledge of MS Office)
  • Aptitude for self-directed learning
  • Good medical knowledge and its application in drug safety
  • Sound understanding of the Drug Safety and Regulatory process
  • Good problem solving and decision-making skills
  • Initiative-taking, able to prioritize and plan effectively
  • Excellent interpersonal and communication skills
  • Team player with ability to function in a multi–disciplinary environment

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