REF 1831048
18.06.2025 | Abu Dhabi | full time
Reviewing and assessing all incoming data for serious adverse effects and product quality complaints
Conducting investigations and preparing safety reports to submit to local and international regulatory authorities
Tracking all adverse event reports received and completed
Ensuring compliance wit.
Applicants 11
REF 1912271
10.10.2025 | Abu Dhabi | full time
They determine from the data whether the medicine is safe and effective enough to proceed into the next phase of research or to apply for its approval. Companies also carry out ongoing pharmacovigilance (Phase IV trials) through healthcare professionals and consumers.
Applicants 2
REF 1906307
02.10.2025 | Dubai | full time
working in local and global projects within the Pharmacovigilance (PV) and Safety department and opportunity to work in all aspects of pharmacovigilance, such as handling adverse events, writing of aggregate reports, maintenance of the Pharmacovigilance system, implementing Risk Management Plans.
Applicants 2
REF 1905303
30.09.2025 | Abu Dhabi | full time
As a Senior Pharmacovigilance Officer you will evaluate the safety data for assigned products, contribute to development risk management plans and signal detection in collaboration with the GSO.
Applicants 2
REF 1904817
30.09.2025 | Dubai | full time
As a Senior Pharmacovigilance Officer, you will be required to: Provide first inspection of individual case safety reports (ICSRs) Conduct Document Control, surrounding the adverse effects of a released drug product. Maintain the SOPs.
Applicants 2
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