Pharmacovigilance Medical Reviewer

Tata Consultancy Services; Ciudad de México; Presencial; MXN 380.000 - 520.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Major Medical Insurance

Life Insurance

Grocery Vouchers

Christmas Bonus

Vacation days (Mexican labor law)

Descripción de la vacante

TATA Consultancy Services in Mexico City is seeking a Medical Reviewer to support medical review and assessment of adverse event reports, ensuring accuracy, quality, and regulatory compliance in pharmacovigilance activities. The role collaborates with Drug Safety teams and cross-functional stakeholders to evaluate safety data throughout the product lifecycle.

The candidate will review safety narratives, medical history, and lab data, assess causality and seriousness, and respond to safety

Formación

• Bachelor of Medicine and Bachelor of Surgery (MBBS) or equivalent medical degree.
• 9 months to 4 years of experience in Pharmacovigilance, Drug Safety, Clinical Research, or related fields.
• Strong communication skills in English.
• Availability for full-time employment.

Responsabilidades

• Perform medical review and assessment of adverse event and drug safety cases.
• Evaluate case narratives, laboratory data, medical history, concomitant medications, and suspect products.
• Assess medical causality, seriousness, and labeling relevance of safety cases.
• Review and respond to queries related to individual case safety reports.
• Generate and track medically relevant follow-up requests for additional safety information.
• Support Drug Safety teams with medical expertise and product-related knowledge.
• Ensure compliance with regulatory requirements, SOPs, and pharmacovigilance processes.
• Participate in audits, safety reviews, and stakeholder discussions.

Conocimientos

Communication skills

English proficiency

Educación

MBBS or equivalent medical degree

Descripción del empleo

TATA Consultancy Services in Mexico City is seeking a Medical Reviewer to support medical review and assessment of adverse event reports, ensuring accuracy, quality, and regulatory compliance in pharmacovigilance activities. The role collaborates with Drug Safety teams and cross-functional stakeholders to evaluate safety data throughout the product lifecycle.

The candidate will review safety narratives, medical history, and lab data, assess causality and seriousness, and respond to safety