ICSR case processing || SPE/SME

2coms; Bengaluru Urban; On-site; INR 600,000 - 900,000; Full time

Job summary

2coms is seeking a Process Executive / Subject Matter Expert / Team Leader in Bangalore North, India. The role involves data entry, narrative writing, and pharmacovigilance case processing using Veeva Safety and/or Argus Safety systems. It requires 1–10 years of PV experience and a life sciences or related degree.

The position is full-time with potential team-lead responsibilities and strong emphasis on timely documentation and cross-functional collaboration in a global setting.

Qualifications

• 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.

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

Communication skills

Presentation skills

Intercultural work

Education

Life Sciences/Pharmacy/Medical Sciences degree

Tools

Veeva Safety

Argus Safety

Job description

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

• Industry Pharma/Biotech/Clinical Research

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