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Job Description
- Training the employees of the company on the concept of drug vigilance and importance and how to deal with adverse reactions, recording and informing the QPPV.
- For product re-registration, RMP (Risk Management plan report) & ACO (Addendum of clinical overview) should be submitted to EPVC (Egyptian pharmacovigilance center).
- Having an overview of the safety profiles and any emerging safety concerns to the company's drugs.
- Preparing SOP for pharma co-vigilance practice & any related company information.
Job Requirements
- BSc. of Science / Pharmacy.
- 1-2 years of experience in regulatory affairs.
- Very good English & Computer skills.
- Having very good communication & presentation skills.
