Wanted Pharmacovigilance Case Processing Trainee -Madurai

Resolve Medicode; Theni, Dindigul, Madurai District; On-site; INR 200,000 - 320,000; Full time

Job summary

Resolve Medicode invites motivated freshers to join its Pharmacovigilance team in Tamil Nadu. You will receive extensive training in drug safety, adverse event reporting, case processing, medical terminology, and safety data management while supporting day-to-day pharmacovigilance activities.

Ideal candidates hold MBBS/BDS/BHMS/BAMS/BSMS/Pharmacy or related life sciences degrees, with 2025-2026 pass-outs welcome.

Qualifications

• MBBS/BDS/BHMS/BAMS/BSMS/PHARMACY graduates may apply.
• Life sciences or biology degrees also eligible for pharmacovigilance support.
• Freshers with relevant coursework welcome; 2025-2026 passed out is indicated.

Responsibilities

• Assist in collecting and processing adverse event reports.
• Review patient safety information for completeness and accuracy.
• Enter safety data into pharmacovigilance databases.
• Perform basic assessment of seriousness and validity of safety cases.
• Assist in follow-up activities for missing case information.
• Perform quality checks on safety cases and resolve data discrepancies.
• Ensure assigned tasks are completed within quality and timeline requirements.

Skills

Medical terminology

Attention to detail

Analytical skills

Written & verbal communication

Education

MBBS

BDS

BHMS

BAMS

BSMS

PHARMACY

BSc Life Sciences

MSc Life Sciences

B.E Biomedical

B.Tech Biotechnology

Job description

Job Summary:

We are looking for motivated freshers to join our Pharmacovigilance team. The candidate will receive training in drug safety processes, adverse event reporting, case processing, medical terminology, and safety data management while supporting day-to-day pharmacovigilance activities.

Qualification & Specifications:

MBBS,BDS,BHMS,BAMS,BSMS,PHARMACYB.Sc/M.Sc (Life Sciences / Biology / Bio Chemistry / Micro Biology / Nursing / Bio Technology), B.P.T, B.E BIOMEDIAL, B.Tech (Biotechnology/Bio Chemistry).

2025 -2026 passed out

Key Responsibilities:

• Assist in collecting and processing adverse event reports.
• Review patient safety information for completeness and accuracy.
• Enter safety data into pharmacovigilance databases.
• Perform basic assessment of seriousness and validity of safety cases.
• Assist in follow-up activities for missing case information.
• Perform quality checks on safety cases and resolve data discrepancies.
• Ensure assigned tasks are completed within quality and timeline requirements.

Skills Required:

• Good understanding of medical terminology.
• Strong attention to detail.
• Good analytical and problem-solving skills.
• Good written and verbal communication.