Wanted Pharmacovigilance Assistant- Bangalore

Resolve Medicode; Krishnagiri District; On-site; INR 240,000 - 420,000; Full time

Job summary

Resolve Medicode invites fresh graduates to join its Pharmacovigilance team. You 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.

We welcome MBBS, BDS, BHMS, BAMS, BSMS, PHARMACY, and related life sciences graduates to apply for this training-focused role and start a career in drug safety.

Qualifications

• MBBS or allied degrees are eligible for entry-level pharmacovigilance.
• Fresh graduates (2025-2026 passed out) can apply for training.
• Strong medical terminology understanding and accurate data entry.

Responsibilities

• Assist in collecting and processing adverse event reports.
• Review 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

Verbal and written communication

Education

MBBS

BDS

BHMS

BAMS

BSMS

PHARMACY

B.Sc / M.Sc (Life Sciences / Biology / Bio Chemistry / Micro Biology / Nursing / Bio Technology)

B.P.T

B.E / BIOMEDICAL

B.Tech (Bi Biotechnology/Bio Chemistry)

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.