Wanted Pharmacovigilance Assistant- Bangalore

Resolve Itech Corp; Krishnagiri District, Bengaluru; On-site; INR 180,000 - 300,000; Full time

Job summary

Resolve Itech Corp in Tamil Nadu invites fresh graduates to join our Pharmacovigilance team. You will receive comprehensive training in drug safety processes, adverse event reporting, case processing, medical terminology, and safety data management, while supporting daily pharmacovigilance activities.

The role focuses on collecting reports, validating data, and ensuring timely, accurate entry and quality checks across safety databases, with mentorship and growth opportunities for 2025–2026

Qualifications

• 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 BIOMEDIAL, B.Tech (Biotechnology/Bio Chemistry).
• 2025 - 2026 passed out

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 and verbal 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 BIOMEDIAL

B.Tech (Biotechnology/Bio Chemistry)

2025 - 2026 passed out

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, PHARMACY B.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.