REF 1905498
30.09.2025 | Abu Dhabi | full time
- General
- Location: Abu Dhabi
- Occupancy: full time
- Description
- Adverse Event (AE) Management: Receive, document, and assess AE reports and product complaints for pharmaceutical products.
Regulatory Reporting: Submit AEs to regulatory authorities, such as the Ministry of Health and Prevention (MoHAP) in the UAE, within mandated timelines.
Database Management: Maintain a compliant Pharmacovigilance System Master File (PSMF).
Regulatory Liaison: Serve as a key contact for pharmacovigilance (PV) communication and inspections by health authorities.
Cross-functional Collaboration: Work with departments like Regulatory Affairs, Quality Assurance, and Medical Affairs.
Safety Monitoring: Conduct local literature reviews and signal detection to monitor product safety.
Compliance: Ensure adherence to national and international pharmacovigilance regulations and internal standard operating procedures (SOPs).
Training: Train internal teams on PV reporting procedures and best practices.
Inspection Support: Assist with internal audits and regulatory inspections.
Report Preparation: Prepare and submit safety reports, updates, and follow-up documents as per regulatory guidelines
- Requirements
- Experience: 3 years
- Bachelor degree
- CV
- Provisions
- Salary: to be discussed
- Employment visa provided
- Transportation provided
- Housing provided
- Medical insurance provided
- Publisher
- direct employer
- 51 - 200 employees