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ICON plc is a world-leading healthcare intelligence and clinical research organization.
We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
What You Will Do
You will take ownership of pharmacovigilance and drug safety deliverables, applying your expertise to complex challenges.
Key Responsibilities
Leading the collection, evaluation, and processing of adverse event reports to ensure timely and accurate reporting in accordance with regulatory guidelines and company policies.
Conducting thorough data analysis and interpretation of safety data, identifying trends and potential safety signals that require further investigation.
Preparing and submitting comprehensive periodic safety update reports (PSURs) and other regulatory documents, ensuring compliance with international regulations.
Collaborating with medical and clinical teams to assess the clinical relevance of reported adverse events and contribute to risk management activities.
Overseeing the maintenance and integrity of pharmacovigilance databases, ensuring accurate documentation and compliance with data management standards.
Providing training and mentorship to junior team members on pharmacovigilance processes, regulatory requirements, and best practices.
Engaging in audits and inspections conducted by regulatory authorities, ensuring readiness and compliance with all relevant pharmacovigilance requirements.
Your Profile
You will have a strong foundation in pharmacovigilance and drug safety, with the experience to work independently and guide others.
Required Qualifications And Experience
Bachelor's degree in a relevant scientific discipline or healthcare-related field
Extensive experience in pharmacovigilance or drug safety,



with a strong understanding of relevant regulations and industry standards.
Proven ability to manage the pharmacovigilance process effectively, including adverse event reporting and signal detection.
Strong analytical and critical thinking skills, with the ability to interpret complex data and make informed recommendations.
Advanced level of English
Based in Buenos Aires - 100% Remote
What ICON Can Offer You
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.
Our Benefits Examples Include
Various annual leave entitlements
A range of health insurance offerings to suit you and your family's needs.
Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
Integral Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being.
Life assurance
Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
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 you need a reasonable accommodation due to a medical condition or disability for any part of the application process, or in order to perform the essential functions of a position, please let us know.
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Postúlate en Kit Empleo: kitempleo.com.ar/empleo/q5t9w

📌 Senior Pharmacovigilance Associate (Buenos Aires)
🏢 Nextrials
📍 Buenos Aires