About the role
As a Pharmacovigilance Associate, you will be responsible for the evaluation, monitoring, and reporting of adverse drug reactions. Your role involves collaborating with healthcare professionals to ensure compliance with safety regulations and quality standards. This position is ideal for those looking to grow in a dynamic environment focused on patient safety.
You will work closely with cross-functional teams, providing insights and contributing to the preparation of safety reports. If you have a strong background in pharmacovigilance and a passion for improving healthcare outcomes, we invite you to apply.
What you'll do
- Evaluate and monitor safety data for adverse drug reactions
- Prepare and submit safety reports to regulatory authorities
- Collaborate with healthcare professionals to ensure compliance
What you'll need
- Bachelor's degree in Pharmacy or Life Sciences
- 2+ years of experience in pharmacovigilance
- Strong analytical and communication skills
Skills
Knowledge of pharmacovigilance regulations
Strong attention to detail
Excellent communication skills
Good to have
Familiarity with safety databases
Project management experience
Benefits
- Competitive salary package
- Health insurance coverage
- Opportunities for professional development
Interested in this role?
It takes about two minutes. Free to apply — Callabri never asks candidates for money.
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Questions about this job
What are the key responsibilities of this role?
You will evaluate and monitor adverse drug reactions, collaborate with healthcare professionals, and prepare safety reports.
Is there a specific qualification required?
A degree in Pharmacy, Life Sciences, or related fields is preferred.
What is the work schedule for this position?
This is a full-time onsite role, typically following standard office hours.
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