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Job Description
- Day to day adverse event, incident and pregnancy cases reporting.
- Responsible for PV documents submission to Egyptian Pharmaceutical Sciences centre
- Create and maintain Local SOP for Pharmacovigilance.
- Maintain local Pharmacovigilance master file.
- Monitor Local Regulations.
- Develop and follow up on Risk management plans.
- Conduct training on adverse events reporting.
- Conduct local Literature search in international databases and maintain list of local journals.
- Regular review of Product Complaints and Medical information enquiries to ensure that Adverse Events associated with product complaints and medical information enquiries has been reported.
- Exchange of safety data with third parties and conducting annual compliance check.
- Respond to local regulatory authorities queries and requests and Central Safety Department requests
Job Requirements
- Bachelor degree in Pharmaceutical Sciences
- Excellent communication, negotiation and organization skills.
- Strong interpersonal skills with good communication skills
- Excellent command of the English language
- Effective presentation skills
- Good Computer skills (Word, Excel & PowerPoint).