NEW
REF 1831048
32 hours ago | Abu Dhabi | full time
General
Location: Abu Dhabi
Occupancy: full time
Description
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 with standard operating procedures and working instructions
Providing training to staff on pharmacovigilance activities
Keeping up-to-date with pharmacovigilance regulations and guidelines
Collaborating with other departments to establish proper protocols and procedures
Requirements
Experience: 1 year
Bachelor degree
CV
Provisions
Salary: to be discussed
Employment visa provided
Transportation provided
Housing provided
Medical insurance provided
Publisher
FORCE 10 UAE LLC
direct employer
more than 200 employees