Job Title:
Senior Pharmacovigilance Associate
Employer:
ICON Strategic Solutions
Location:
Brazil (Remote / Homeworking)
Start Date:
24 October 2025
Closing Date:
23 November 2025
Salary:
Competitive
About ICON Strategic Solutions:
ICON plc is a world-leading healthcare intelligence and clinical research organization. We are proud to foster an inclusive and innovative environment that drives excellence in clinical development. At ICON, we are on a mission to shape the future of healthcare by accelerating the development of life-changing medicines and improving patient outcomes.
Position Overview:
We are seeking an experienced Senior Pharmacovigilance Associate to join our global pharmacovigilance team.
In this role, you will be responsible for managing and overseeing pharmacovigilance activities to ensure product safety, compliance with regulatory requirements, and protection of patient health.
You will collaborate with cross-functional teams, support audits, and provide mentorship to junior colleagues while maintaining high-quality safety data standards.
Key Responsibilities:
Safety Case Management
Lead the collection, evaluation, and processing of Adverse Event (AE) reports according to regulatory and company timelines.
Conduct detailed safety data analysis, identifying trends, potential safety signals, and areas requiring further investigation.
Ensure timely submission of Periodic Safety Update Reports (PSURs) and other regulatory safety documentation.
Collaboration and Medical Support
Partner with medical and clinical teams to assess the clinical relevance of reported adverse events.
Contribute to risk management and signal detection activities.
Provide medical and scientific input during internal and external meetings.
Process Oversight & Compliance
Oversee pharmacovigilance databases to maintain data integrity and accuracy.
Ensure compliance with Good Pharmacovigilance Practices (GVP) and all applicable regulatory standards.
Participate in audits and inspections by health authorities, ensuring readiness and adherence to PV regulations.
Leadership & Mentorship
Train and mentor junior team members in pharmacovigilance processes and documentation best practices.
Promote continuous improvement by staying informed on evolving regulations and integrating industry best practices into team operations.
Your Profile:
Bachelor’s degree in Life Sciences, Pharmacy, Nursing, or a related field (advanced degree preferred).
Extensive experience in pharmacovigilance or drug safety, with solid understanding of global PV regulations and reporting standards.
Proven ability to manage PV processes, including case handling, signal detection, and aggregate reporting.
Strong analytical and critical-thinking abilities for interpreting complex safety data.
Excellent communication and interpersonal skills for cross-functional collaboration.
Proficiency in pharmacovigilance databases (e.g., Argus, ARISg) and Microsoft Office Suite.
Ability to work independently, handle multiple projects, and meet deadlines in a fast-paced environment.
High level of confidentiality and professionalism when handling patient data.
What ICON Offers:
At ICON, we recognize that our success depends on our people. We’ve built a diverse culture that rewards performance, supports professional development, and encourages work-life balance.
Benefits Include:
Competitive salary and comprehensive annual leave entitlements.
Wide range of health insurance options for you and your family.
Retirement planning programs to help you secure your financial future.
Global Employee Assistance Programme (LifeWorks): 24/7 access to 80,000+ specialists for well-being support.
Life assurance coverage.
Flexible country-specific benefits such as:
Childcare vouchers
Bike purchase schemes
Gym membership discounts
Subsidized travel passes
Health assessments and more
🔗 Explore ICON’s benefits: https://careers.iconplc.com
Diversity, Inclusion & Equal Opportunity:
At ICON, inclusion and belonging are central to our values. We are committed to maintaining a discrimination-free workplace and providing equal opportunities for all candidates.
All qualified applicants will be considered regardless of race, color, religion, sex, gender identity, sexual orientation, national origin, disability, or veteran status.
If you require reasonable accommodation for a disability or medical condition during the application or work process, please contact us through the ICON careers site.
Application Information:
If you are dedicated to ensuring patient safety and compliance in pharmacovigilance, we invite you to apply.
Even if you don’t meet every requirement, we encourage you to submit your application—you may be exactly the candidate we’re looking for.
🔗 Apply via ICON Careers Portal: https://careers.iconplc.com
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