REF 1871075
12.08.2025 | Dubai | full time
General
Location: Dubai
Occupancy: full time
Description
Developing and maintaining pharmacovigilance procedures and protocols.
Conducting safety analysis and signal detection.
Participating in pharmacovigilance inspections and audits.
Training staff on pharmacovigilance procedures and regulations.
Reviewing and contributing to clinical trial protocols and safety reports.
Recording and reporting adverse reactions received from healthcare professionals, drug company representatives and patients.
Conducting in-depth interviews with patients.
Developing thorough knowledge of products.
Conducting safety update reports on drugs and other treatments.
Writing and reviewing serious adverse effects reports and forms for the pharmacovigilance departments of pharmaceutical firms.
Monitoring all products and conducting post-market evaluations to ensure drug safety.
Assessing adverse event writings, updating reports on safety, conducting quality and conveying drug related case reports to appropriate authorities.
Requirements
Ability to keep meticulous records
Passion for detail
Meticulous approach to work
Excellent analytical and problem-solving skills
Ability to interact and communicate effectively with a wide range of people
A systematic approach to tasks
Excellent IT skills
Good interpretative skills
Ability to work in teams
Good at maths
Provisions
Salary: to be discussed
Employment visa provided
Publisher
direct employer
more than 200 employees