EVERSANA is inviting applications from experienced Pharmacovigilance and Drug Safety professionals for multiple fully remote opportunities across India. Shortlisted candidates will be invited for an in-person interview in Chandigarh.

These openings include Safety Writing Specialist, Lead Safety Operations, Medical Reviewer, and Lead Medical Reviewer positions. Professionals with experience in Aggregate Report Writing, Pharmacovigilance Operations, ICSR Medical Review, and Project Leadership are encouraged to apply.

If you’re looking for remote pharmacovigilance jobs in India, this is an excellent opportunity to work with a global healthcare organization while contributing to high-impact drug safety projects.

About EVERSANA

EVERSANA is a global provider of commercial services to the life sciences industry, supporting pharmaceutical, biotechnology, and medical device companies across the entire product lifecycle. The company delivers integrated solutions in pharmacovigilance, regulatory affairs, commercialization, consulting, medical affairs, and patient services.

Available Positions

1. Safety Writing Specialist

Key Responsibilities

• Prepare and manage global aggregate safety reports including:
  • PADER
  • DSUR
  • PSUR/PBRER
  • Annual Safety Reports
  • IND Annual Reports
• Develop Risk Management documents
• Collaborate with global cross-functional teams
• Ensure regulatory compliance and timely submissions
• Maintain high-quality scientific documentation

Eligibility

Qualification

• Graduation in Life Sciences
• Pharm.D
• M.Pharm
• BDS

Experience

• 4–5 years in Aggregate Safety Report Writing preferred

2. Lead Safety Operations

Key Responsibilities

• Lead Pharmacovigilance projects
• Manage end-to-end safety operations
• Allocate project resources
• Ensure quality and regulatory compliance
• Handle client communication
• Mentor and develop PV teams
• Support continuous process improvement
• Oversee case processing activities

Eligibility

Qualification

• Pharm.D
• M.Pharm
• BDS

Experience

• 5+ years
• Project leadership experience preferred

3. Medical Reviewer

Key Responsibilities

• Perform medical review of clinical trial and post-marketing ICSRs
• Conduct medical assessment and causality evaluation
• Review expectedness and seriousness
• Ensure MedDRA coding accuracy
• Review case narratives
• Support signal management
• Contribute to aggregate safety reporting
• Ensure global regulatory compliance

Eligibility

Qualification

• MBBS
• MD

Experience

• 3–5 years as Medical Reviewer handling ICSRs

4. Lead Medical Reviewer

Key Responsibilities

• Lead Medical Review teams
• Mentor and guide reviewers
• Ensure quality and compliance
• Manage client projects
• Support pharmacovigilance strategy
• Oversee complex medical assessments
• Manage project delivery and resource planning

Eligibility

Qualification

• MBBS
• MD

Experience

• 5+ years as Medical Reviewer
• 1–2 years project leadership experience

Job Highlights

• Company: EVERSANA
• Employment Type: Full-Time
• Work Mode: Fully Remote
• Interview Mode: Face-to-Face
• Interview Location: Chandigarh
• Interview Date: 20 July 2026
• Functional Area: Pharmacovigilance
• Industry: Life Sciences

Why Join EVERSANA?

• 100% Remote Working Opportunity
• Global Pharmacovigilance Exposure
• Aggregate Safety Reporting Projects
• Leadership Opportunities
• International Client Interaction
• Career Growth in Drug Safety
• Cross-functional Learning Environment

How to Apply

Interested candidates should email their updated resume with the following subject format:

Position Name – Your Name – Years of Experience – Current Location

Email: priyanka.gupta2@eversana.com

Only shortlisted candidates will be invited for the Face-to-Face Interview in Chandigarh.

Important Dates