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This role oversees the safety monitoring and reporting of adverse events related to clinical trials and marketed products at ICON. You will lead a pharmacovigilance team, ensuring compliance with regulatory requirements and optimizing processes in collaboration with other departments.
ICON plc
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At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise.
As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.
As a Supervisor, Pharmacovigilance at ICON, you will oversee the safety monitoring and reporting of adverse events related to clinical trials and marketed products.
What You Will Do:
You will manage day-to-day pharmacovigilance and drug safety activities, supporting your team to deliver quality outcomes.
Key responsibilities include:
Your Profile:
You will have solid pharmacovigilance and drug safety experience, with the ability to manage competing priorities and develop your team.
Required qualifications and experience:
Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
Rewards & Benefits
ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.
Benefits may include:
Benefits may vary depending on role and location.
Visit our careers site to read more about the benefits ICON offers.
Inclusion and Accessibility
ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.
If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.
Are you a current ICON Employee? Please click here to apply
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