ICSR case processing || SPE/SME

2coms; Bangalore Rural; On-site; INR 600,000 - 1,200,000; Full time

Job summary

2coms is seeking a Process Executive / SME / Team Leader for pharmacovigilance work in Bangalore North, India. The role emphasizes safety case processing with hands-on use of Veeva Safety and Argus Safety.

The position requires 1–10 years of PV experience and offers full-time employment. You will handle data entry, narrative writing, coding, QC checks, and timely case closures while collaborating across teams.

Qualifications

• Experience in pharmacovigilance safety case processing.
• Proficiency with medical coding and clinical data entry.
• Strong written and verbal communication.

Responsibilities

• Book-in and full data entry
• Narrative writing / I-Narrative
• Medical coding & Product coding
• Self-check using Online QC Tool
• Unblinding (if required)
• Case routing
• Case lock/closure (where applicable)
• USPI labeling

Skills

Data entry

Narrative writing

Medical coding

Case routing

Unblinding

Veeva Safety

Argus Safety

Intercultural communication

Presentation skills

Education

Graduate/Postgraduate/Doctorate in Life Sciences, Pharmacy, Medical Sciences, or equivalent

Tools

Veeva Safety

Argus Safety

Job description

Bangalore North, India | Posted on 08/20/2026

• Industry Pharma/Biotech/Clinical Research
• Dial in Number [phone]
• Dial in Extension to connect with Recruiter 404

Job Description

About the Company:

Our client is a leading Global Fortune 500 IT solutions company that specializes in providing simple and scalable solutions to solve complex business challenges. With a workforce of over 500,000 employees, they offer technical and domain expertise across various platforms and industries to assist enterprise companies in enhancing productivity, efficiency, and optimizing their technology investments.

Position Title: Process executive / Subject matter expert/ Team Leader

Experience Required:-1-10 Years (For TL - on paper 2yrs)

Employment Type: Full-Time

Key Responsibilities:

• Book-in and full data entry
• Narrative writing / I-Narrative
• Medical coding & Product coding
• Self-check using Online QC Tool
• Unblinding (if required)
• Case routing
• Case lock/closure (where applicable)
• USPI labeling
• Graduate/Postgraduate/Doctorate in Life Sciences, Pharmacy, Medical Sciences, or equivalent
• 1–10 years of Pharmacovigilance Safety Case Processing experience
• Hands-on experience with Veeva Safety and/or Argus Safety databases

Requirements

• Relevant educational background and experience in patient safety or related field
• Strong presentation and communication skills
• Effective intercultural work capabilities
• Commitment to timely completion of tasks and documentation