NEW
REF 1831645
20 hours ago | Abu Dhabi | full time
- General
- Location: Abu Dhabi
- Occupancy: full time
- Description
- Collect, organize and assess data on the safety and efficacy of drugs from clinical trials, healthcare providers, patients, and other sources
Identify and evaluate potential adverse reactions to a drug, including their severity and frequency
Prepare and submit periodic safety update reports to regulatory authorities
Conduct signal detection activities for proactive risk identification
Investigate any drug-related problems and propose corrective actions
Participate in the development and implementation of risk management plans
Ensure compliance with pharmacovigilance regulations and guidelines
Communicate findings to healthcare professionals, patients, and the public
Liaise with regulatory authorities, healthcare professionals, and pharmaceutical companies to ensure the safety of pharmaceutical products
Maintain an up-to-date knowledge of pharmacovigilance legislation and practice
- Requirements
- Requirements:
At least 3 years of documented PV experience in the pharmaceutical industry/CRO
Life sciences education
Management skills
Good communication skills
Excellent command of Spanish and English
Team player, proactive and quality minded
Ability to work independently and assume responsibilities
- Provisions
- Salary: to be discussed
- Medical insurance
- Publisher
- direct employer
- 50 - 200 employees