ICSR case processing TL

2COMS Consulting Pvt. Ltd.; Mumbai; On-site; INR 1,200,000 - 1,800,000; Full time

Job summary

2COMS Consulting Pvt. Ltd. seeks a Process Executive / Subject Matter Expert / Team Leader for Pharmacovigilance in Mumbai. The role requires 7–12 years of PV safety case processing experience and hands-on work with Veeva or Argus Safety databases.

You will manage data entry, narrative writing, medical/product coding, and QC checks, with attention to timely documentation and cross-functional collaboration.

Qualifications

• Graduate/Postgraduate/Doctorate in Life Sciences, Pharmacy, Medical Sciences, or equivalent.
• 7-12 years of Pharmacovigilance Safety Case Processing experience.
• Hands-on experience with Veeva Safety and/or Argus Safety databases.
• Strong English communication skills.

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

Strong English communication skills

Analytical and problem-solving skills

Collaboration and teamwork abilities

Effective intercultural work abilities

Strong presentation and communication

Education

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

Tools

Veeva Safety

Argus Safety

Job description

SUMMARY

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:-7-12 Years (For TL - on paper 2yrs)

Location: Hyderabad/Pune/Mumbai/Bengaluru

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

Eligibility:

• Graduate/Postgraduate/Doctorate in Life Sciences, Pharmacy, Medical Sciences, or equivalent
• 7 12 years of Pharmacovigilance Safety Case Processing experience
• Hands-on experience with Veeva Safety and/or Argus Safety databases
• Strong English communication skills

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
• Analytical and problem-solving skills
• Collaboration and teamwork abilities