About the role
This role involves analyzing adverse event reports, conducting literature reviews, and ensuring compliance with regulatory requirements. The ideal candidate will have a background in life sciences and experience in pharmacovigilance processes. You will work closely with cross-functional teams to ensure data integrity and timely reporting of safety information. This position is perfect for individuals looking to advance their career in the pharmaceutical industry while contributing to patient safety.
What you'll do
- Analyze and report adverse event data
- Conduct literature reviews for safety information
- Ensure compliance with regulatory requirements
- Collaborate with cross-functional teams
What you'll need
- Degree in life sciences or related field
- 2-5 years of experience in pharmacovigilance
- Strong analytical skills
Skills
Knowledge of pharmacovigilance processes
Strong attention to detail
Excellent communication skills
Good to have
Familiarity with regulatory guidelines
Experience with safety databases
Benefits
- Competitive salary
- Health insurance coverage
- Professional development opportunities
Interested in this role?
It takes about two minutes. Free to apply — NodHire never asks candidates for money.
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Questions about this job
What are the key responsibilities of a Pharmacovigilance Associate?
You will analyze adverse events, ensure compliance with regulations, and collaborate with different teams.
What qualifications do I need for this role?
A degree in life sciences and experience in pharmacovigilance are required.
Is this position remote or onsite?
This is an onsite position in Gurugram.
What is the salary range for this role?
The salary ranges from ₹50,000 to ₹80,000 monthly.
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