About the role
In this role, you will assist in monitoring the safety of pharmaceutical products by collecting and analyzing adverse event reports. Your work will contribute to the overall assessment of drug safety and regulatory compliance. This is an excellent opportunity for those interested in pharmacovigilance and drug safety.
You will collaborate with cross-functional teams to ensure that all safety data is accurately recorded and reported as required. Ideal candidates will have a background in life sciences and a strong attention to detail. If you are eager to enhance your skills in a supportive environment, we invite you to apply.
What you'll do
- Monitor drug safety
- Collect and analyze adverse event reports
- Ensure compliance with regulatory requirements
- Assist in preparing safety reports
What you'll need
- Bachelor's degree in Life Sciences
- 1-3 years of experience in pharmacovigilance or related field
- Strong analytical skills
Skills
Analytical skills
Attention to detail
Communication skills
Good to have
Knowledge of safety databases
Familiarity with regulatory guidelines
Benefits
- Competitive pay
- Work-life balance
- Professional development opportunities
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 main duties of a Pharmacovigilance Associate?
You will collect and analyze safety data and assist with reporting adverse events.
Can fresh graduates apply?
Click "Apply Now" on this page to apply through Callabri. Callabri is recruiting for this role on behalf of a client employer.
What is the work schedule for this part-time role?
The working hours are flexible and can be discussed during the interview.
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