RENEWED: 3 hours ago
REF 1875615
19.08.2025 | Abu Dhabi | full time
- General
- Location: Abu Dhabi
- Occupancy: full time
- Description
- Monitoring and Reporting Adverse Events:
Pharmacovigilance Officers are responsible for identifying, collecting, and analyzing information about adverse drug reactions (ADRs) and other safety-related issues from various sources like clinical trials, spontaneous reports, and literature.
Risk Management:
They contribute to the development and implementation of risk management plans to minimize potential harm from medications.
Compliance with Regulations:
Ensuring that the company adheres to all relevant pharmacovigilance regulations and guidelines set by regulatory bodies.
Reporting to Authorities:
Preparing and submitting safety reports to regulatory agencies, such as the FDA, EMA, or other relevant authorities.
Collaboration:
Working with other departments, such as medical affairs, clinical development, and regulatory affairs, as well as with external stakeholders like healthcare professionals and patients.
Signal Detection and Evaluation:
Participating in signal detection activities to identify potential new safety concerns associated with medications.
Medical Writing:
Preparing various pharmacovigilance documents, including safety update reports, risk management plans, and regulatory submissions.
Maintaining Safety Databases:
Ensuring accurate and up-to-date records of adverse events and other safety information in company databases.
- Requirements
- Experience: 3 years
- Bachelor degree
- CV
- Provisions
- Salary: to be discussed
- Employment visa provided
- Transportation provided
- Housing provided
- Medical insurance provided
- Publisher
- MISPAH PIPELINE INSPECTION SERVICES L.L.C
- direct employer
- 51 - 200 employees