[Hiring] Pharmacovigilance Assistant @ICON plc

Role Description

As a Pharmacovigilance Assistant I at ICON, you will support the collection, documentation, and reporting of safety data related to medications and clinical trials.

What You Will Do:

• Contribute to pharmacovigilance and drug safety activities, taking responsibility for your deliverables and working collaboratively.
• Support the collection, review, and processing of adverse event reports related to clinical trials and marketed products.
• Ensure timely and accurate data entry of safety information into pharmacovigilance databases.
• Assist in the preparation and submission of safety reports to regulatory authorities and sponsors, as required.
• Collaborate with cross-functional teams to maintain compliance with safety regulations and company protocols.
• Maintain detailed records and documentation related to pharmacovigilance activities and safety reporting.

Qualifications

• Bachelor's degree in life sciences, pharmacy, or a related field.
• Basic understanding of pharmacovigilance principles and regulatory requirements is preferred.
• Strong attention to detail and organizational skills, with the ability to manage multiple tasks efficiently.
• Effective communication and collaboration skills, with a focus on maintaining accuracy in documentation and reporting.
• Ability to work in a fast-paced, regulated environment, ensuring compliance with safety guidelines and protocols.

Requirements

• Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

Benefits

• Competitive base salary and performance related incentives.
• Health and wellbeing programmes including medical, dental, and vision coverage where applicable.
• Retirement and pension plans.
• Life assurance and disability coverage.
• Employee assistance programmes and wellbeing resources.
• Learning and development opportunities through structured training and career pathways.
• Benefits may vary depending on role and location.