REF 1517197
28.04.2024 | Dubai | full time
- General
- Location: Dubai
- Occupancy: full time
- Description
- Requires strong attention to detail in composing and proof-reading materials,
establishing priorities, scheduling and meeting deadlines.
- Requirements
- Experience: 3 years
- Bachelor degree
- Knowledge of global regulations and guidance related to Post marketing studies
Pharmacovigilance, risk management
• Experience in: review of serious adverse event (SAE) reports received from post
marketing sources for review; regulatory compliance during pharmacovigilance of
the new drug; expedited safety reports, or periodic safety reports during clinical
research; assist project management activities related to drug safety
• Working knowledge of MedDRA terminology and practices.
• Ability in solving problems and achieving objectives.
• Ability to work with interdisciplinary, highly matrixed team
• Proficiency with electronic search engines of the medical literature.
- Provisions
- Salary: to be discussed
- Employment visa provided
- Transportation provided
- Housing provided
- Medical insurance provided
- Publisher
- direct employer
- more than 200 employees