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ICON Strategic Solutions is seeking a Pharmacovigilance professional to manage adverse event data collection, review, and processing in line with regulatory requirements. You will assist in preparing safety reports and collaborate with cross-functional teams to ensure timely communication of safety information.
The role involves contributing to PV documentation, SOPs, safety management plans, and participating in ongoing training to strengthen regulatory knowledge.
You will take responsibility for pharmacovigilance and drug safety deliverables, applying your skills to ensure quality and efficiency.
You will bring relevant pharmacovigilance and drug safety experience, along with the following qualifications and skills.
Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here