ICSR case processing | SPE/SME

2COMS Consulting Pvt. Ltd.; Bengaluru Urban; On-site; INR 600,000 - 900,000; Full time

Job summary

2COMS Consulting Pvt. Ltd. in Bangalore is seeking candidates for Process Executive / Subject Matter Expert / Team Leader roles in Pharmacovigilance.

Key tasks include data entry, narrative writing, medical/product coding, QC checks, and case routing. Requires 1–10 years in pharmacovigilance safety case processing and hands-on experience with Veeva Safety or Argus Safety databases. Educational background in Life Sciences or Pharmacy is essential, with strong presentation and intercultural

Qualifications

• Bachelor's or higher in Life Sciences, Pharmacy or Medical Sciences.
• Strong presentation and communication skills.
• Effective intercultural collaboration and documentation.

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

Intercultural collaboration

Data entry

Education

Bachelor/Master in Life Sciences or Pharmacy

Tools

Veeva Safety

Argus Safety

Job description

Bangalore North, India

• 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