Collection, documentation, and reporting of safety data
Adverse event reports processing
Safety information data entry
You will support the collection, documentation, and reporting of safety data related to medications and clinical trials
Job Summary
You will support the collection, documentation, and reporting of safety data related to medications and clinical trials.
Key responsibilities include supporting the collection, review, and processing of adverse event reports related to clinical trials and marketed products.
ICON offers a range of additional benefits designed to be competitive within each country and focused on well-being and work life balance opportunities.
Matching Summary
You will support the collection, documentation, and reporting of safety data related to medications and clinical trials.
Skills & Requirements
Must-have
collection, documentation, and reporting of safety data
adverse event reports processing
safety information data entry
preparation and submission of safety reports
maintaining detailed records and documentation
Nice-to-have
foster an inclusive environment
driving innovation and excellence
collaborative work environment
Key Requirements
Bachelor's degree in life sciences, pharmacy, or related field
Basic understanding of pharmacovigilance principles
Regulatory requirements understanding
Strong attention to detail and organizational skills
Ability to manage multiple tasks efficiently
Effective communication and collaboration skills
Ability to work in a fast-paced, regulated environment