EVERSANA Hiring experienced Pharmacovigilance Professionals – Fully Remote
Are you seeking remote pharmacovigilance jobs in India, aggregate safety writing vacancies, or medical reviewer careers? Leading commercial services provider to the life sciences industry EVERSANA has announced multiple job openings for experienced drug safety professionals under a 100% remote (Work from Home) model, with face-to-face screening rounds organized in Chandigarh.
This medical evaluation, aggregate report writing (PADER, DSUR, PSUR), safety operations project leadership, and ICSR medical review recruitment is open to science, medical, and pharmacy graduates. The positions accept B.Pharm, M.Pharm, Pharm.D, B.Sc, M.Sc, BDS, MBBS, and MD degrees. Depending on the specific role, candidates must possess between 3 to 5+ years of relevant drug safety experience. Shortlisted candidates must attend an in-person, face-to-face interview on 20 July 2026 in Chandigarh. To learn how to structure your scientific writing milestones, aggregate reports exposure, or medical causality assessments in your resume, check our guide on how to apply for healthcare and pharma jobs online.
📋 Job & Interview Highlights
- Company: EVERSANA
- Job Locations: Fully Remote (Work From Home, India)
- Interview Mode: Face-to-Face (In-Person)
- Interview Location: Chandigarh
- Interview Date: 20 July 2026
- Employment Type: Full-Time
- Functional Area: Pharmacovigilance (PV)
💼 Available Openings & Qualifications
-
1. Safety Writing Specialist
Experience: 4 – 5 Years in Aggregate Safety Writing
Qualification: Life Sciences Graduate | Pharm.D | M.Pharm | BDS
Key Duties: Prepare and manage global aggregate safety reports (PADER, DSUR, PSUR/PBRER, IND annual reports) and compile risk management documents. -
2. Lead Safety Operations
Experience: 5+ Years (Project leadership experience preferred)
Qualification: Pharm.D | M.Pharm | BDS
Key Duties: Lead PV projects, manage end-to-end safety operations, allocate resources, oversee case processing, and handle client communications. -
3. Medical Reviewer
Experience: 3 – 5 Years as a Medical Reviewer handling ICSRs
Qualification: MBBS | MD
Key Duties: Medical review of clinical trial and post-marketing ICSRs, causality evaluations, expectedness/seriousness checks, and MedDRA coding validations. -
4. Lead Medical Reviewer
Experience: 5+ Years as a Medical Reviewer (1-2 years project leadership)
Qualification: MBBS | MD
Key Duties: Lead and mentor medical review teams, oversee complex medical assessments, manage project delivery, and resource planning.
🎓 Required General Experience & Skills
- Guidelines Knowledge: Strong understanding of GVP (Good Pharmacovigilance Practices) and international regulatory safety timelines.
- Database & Coding: Practical familiarity with drug safety databases (Argus, ArisG) and coding tools (MedDRA, WHO Drug Dictionary).
- Analytical Writing: Expert scientific writing, literature assessment, data compilation, and editing skills.
- Communication: Excellent written and verbal English communication skills for collaborating with global sponsor teams.
To learn about standard regulatory structures, pharmacovigilance operations, and clinical databases, read our detailed Top 100 Pharmacovigilance Interview Questions.
🎁 Why Join EVERSANA?
- 100% remote working model, allowing you to work from home from anywhere in India.
- Gain exposure to complex aggregate safety reports and global safety surveillance projects.
- Collaborate with international pharmaceutical sponsors and global project leads.
- Structured career paths with leadership opportunities in drug safety and medical review.
For professionals interested in exploring standard compensation packages, domain career tracks, and industry values, check our comparison of Pharmacovigilance Salaries in India vs USA.
📝 Resume Tips for EVERSANA Candidates
- Detail Aggregate Report Types: If applying for safety writing, specify the volume of PSURs, DSURs, or PADERs you have authored.
- Highlight Medical Assessment Skills: If applying as a Medical Reviewer, mention your experience with causality evaluations and expectedness reviews.
- Specify Project Scale: For lead positions, detail the size of the team managed and the number of active drug safety projects coordinated.
💬 EVERSANA Pharmacovigilance Interview Questions
- Q1. What is the difference between a PSUR and a DSUR?
Answer Guidance: A DSUR (Development Safety Update Report) is a periodic safety report prepared during the development and clinical trial phase of an investigational drug. A PSUR (Periodic Safety Update Report) is a post-marketing safety report prepared to evaluate the benefit-risk profile of an approved drug. - Q2. How is causality assessed in an Individual Case Safety Report (ICSR)?
Answer Guidance: Causality is evaluated by assessing the temporal relationship between drug administration and the adverse event, checking for dechallenge and rechallenge results, identifying confounding factors (such as co-medications or underlying diseases), and reviewing reference safety information (RSI). - Q3. Explain what a Risk Management Plan (RMP) is.
Answer Guidance: An RMP is a regulatory document that describes a drug's safety profile, details how its risks will be monitored and characterized (pharmacovigilance activities), and outlines risk minimization measures (like label warnings or educational programs) to ensure patient safety.
📖 How to Apply?
Before submitting your application, please read our step-by-step guidance on how to navigate corporate recruitment mailboxes and format your details:
📧 Email Application Process
This is an Email Application. Send your updated resume directly to the recruitment specialist:
- Email Address: priyanka.gupta2@eversana.com
- Email Subject Line Format: Position Name – Your Name – Years of Experience – Current Location
- Note: Only shortlisted candidates will receive an official invitation for the Face-to-Face interview rounds.
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🚀 Launch Free ATS Resume Tool❓ Frequently Asked Questions
Q. Where are these jobs located and is it remote?
Yes, these are 100% remote (work from home) positions within India.
Q. Do I need to travel for the interview?
Yes, only shortlisted candidates will be invited to attend the mandatory face-to-face (in-person) interview rounds on July 20, 2026, in Chandigarh.
Q. How should I submit my application?
Interested candidates must email their resume to priyanka.gupta2@eversana.com using the subject format: Position Name – Your Name – Years of Experience – Current Location.
