Are you an experienced pharmacovigilance professional looking for your next opportunity in drug safety and global patient safety operations? eTeam is currently hiring a Drug Safety Associate / Pharmacovigilance Associate for a leading global pharmaceutical organization in Gurgaon, Delhi NCR.
This is a 1-year Contract-to-Hire (C2H) opportunity offering exposure to global pharmacovigilance processes, Individual Case Safety Report (ICSR) processing, MedDRA coding, narrative writing, and regulatory compliance activities. Professionals with hands-on experience in adverse event case processing and safety databases are encouraged to apply.
Job Details
- Position: Drug Safety Associate / Pharmacovigilance Associate
- Company: eTeam
- Location: Gurgaon, Delhi NCR, India
- Work Mode: Hybrid
- Experience Required: 2-5 Years
- Employment Type: Contract to Hire (1 Year)
- Industry: Pharmaceutical & Life Sciences
- Department: Research & Development
Key Responsibilities
As a Drug Safety Associate, you will:
- Process adverse event reports received from multiple sources.
- Perform case intake, review, and data entry into safety databases.
- Assess case seriousness, expectedness, causality, and outcomes.
- Prepare medically accurate case narratives.
- Perform MedDRA coding of adverse events and medical information.
- Ensure completeness and accuracy of safety data.
- Generate and track follow-up requests for missing information.
- Conduct quality review and case reconciliation activities.
- Support aggregate reporting and regulatory submissions.
- Ensure compliance with ICH guidelines, GVP requirements, and global pharmacovigilance regulations.
Required Qualifications
Candidates should possess:
- Bachelor’s or Master’s degree in Pharmacy, Nursing, Life Sciences, Biotechnology, Public Health, Biochemistry, Biology, Chemistry, Hospital Management, or related healthcare disciplines.
- 2-5 years of pharmacovigilance or drug safety experience.
- Hands-on experience in ICSR processing and adverse event case management.
- Experience in MedDRA coding and narrative writing.
- Knowledge of ICH guidelines and global pharmacovigilance regulations.
- Excellent verbal and written communication skills.
- Ability to work in a fast-paced environment and manage timelines effectively.
Preferred Skills
Experience with any of the following will be advantageous:
- Argus Safety
- ARISg
- Oracle Safety
- Veeva Vault Safety
- Case Processing and Case Reconciliation
- Clinical Safety Operations
- Global Patient Safety Activities
Why Join This Opportunity?
- Work with a leading global pharmaceutical organization.
- Gain exposure to international pharmacovigilance operations.
- Opportunity for contract extension or permanent conversion.
- Hybrid work environment with flexible work arrangements.
- Hands-on experience with global safety databases and regulatory requirements.
- Enhance expertise in ICSR processing, MedDRA coding, and narrative writing.
How to Apply
