Pharmacovigilance Senior Manager – Post Marketing (FSP, Sponsor-Dedicated)
Company: ICON Strategic Solutions
Location: Brazil (Remote / Home-Based)
Employment Type: Full-Time
Experience Level: Senior / Leadership
Start Date: 14 January 2026
Application Deadline: 13 February 2026
Salary: Competitive (Based on Experience and Market Standards)
About ICON Strategic Solutions
ICON plc is a world-leading healthcare intelligence and clinical research organization, partnering with pharmaceutical, biotechnology, and medical device companies to advance clinical development and deliver innovative therapies globally. ICON is committed to fostering an inclusive, high-performance culture where scientific excellence, patient safety, and professional growth are core priorities.
About the Role
ICON Strategic Solutions is seeking an experienced Pharmacovigilance Senior Manager – Post Marketing to lead sponsor-dedicated pharmacovigilance operations within a Functional Service Provider (FSP) model. This leadership role is critical to ensuring robust post-marketing safety surveillance, regulatory compliance, and continuous improvement across global pharmacovigilance activities.
As a senior leader, you will oversee pharmacovigilance teams, guide safety strategy, and collaborate cross-functionally to ensure the highest standards of patient safety and regulatory excellence.
Key Responsibilities
Leadership & Oversight
Lead and manage pharmacovigilance teams or hubs, ensuring timely and compliant processing of adverse events and safety data
Provide strategic oversight of post-marketing pharmacovigilance activities within a sponsor-dedicated model
Mentor, develop, and support team members to maintain high-quality safety deliverables
Safety Governance & Compliance
Ensure compliance with global pharmacovigilance regulations, guidelines, and internal SOPs (ICH, GVP, FDA, EMA)
Develop, implement, and enhance pharmacovigilance policies, procedures, and risk management practices
Support inspection readiness, audits, and health authority interactions related to drug safety
Cross-Functional Collaboration
Partner with clinical operations, regulatory affairs, medical affairs, and sponsor stakeholders to integrate safety data into clinical development and post-marketing strategies
Provide expert input into safety governance, signal management, and benefit-risk evaluation
Data Review & Continuous Improvement
Monitor and analyze safety data trends to identify emerging risks and inform decision-making
Drive continuous improvement initiatives aligned with industry best practices and evolving regulatory expectations
Stay current with global pharmacovigilance regulations and advancements to strengthen safety operations
Qualifications & Experience Required
Education
Bachelor’s degree in Life Sciences, Pharmacy, Medicine, Nursing, or a related discipline
Advanced degree (Master’s, PharmD, PhD) or relevant pharmacovigilance certifications are strongly preferred
Experience
Minimum 8–12 years of experience in pharmacovigilance or drug safety within pharmaceutical, biotech, CRO, or clinical research environments
Proven experience managing pharmacovigilance teams, programs, or regional/global hubs
Demonstrated experience in post-marketing safety surveillance and sponsor-dedicated or FSP models preferred
Skills & Competencies
Strong expertise in global drug safety regulations and reporting requirements
Excellent leadership, stakeholder management, and decision-making capabilities
Strong analytical skills with a data-driven approach to risk assessment
Ability to influence cross-functional and external stakeholders at senior levels
Excellent written and verbal communication skills
Fluency in English (spoken and written)
Why Join ICON?
Fully remote, home-based role with global exposure
Leadership opportunity within a world-class pharmacovigilance organization
Competitive compensation and country-specific benefits
Comprehensive health, wellness, and work-life balance programs
Global career development, learning, and internal mobility opportunities
Inclusive workplace committed to diversity, equity, and belonging
ICON is an equal opportunity employer and is committed to creating an inclusive and accessible workplace. All qualified applicants will receive consideration for employment without regard to race, religion, gender, age, disability, or any other legally protected status.
Apply via thepharmadaily.com to advance your leadership career in pharmacovigilance and contribute to global patient safety with ICON Strategic Solutions.
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Andover | Billerica | Boston | Cambridge | Devens | Lexington | Massachusetts | Medford and Somerville | Rockland |Wisconsin :
Appleton | Kenosha | Pleasant Prairie | Portage | Waukesha |United states :
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Bulgaria | Vedant |Denmark :
Copenhagen | Denmark |Europe :
Europe | France | Latvia | Lendava | Leuven | Poland | Slovenia | Spain |Finland :
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England | Harlow | Leeds | London | Maidenhead | Salt Lake City | Stevenage | Stirling | United Kingdom |North Yorkshire :
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Tartu | Estonia |Harju County (Maakond) :
Tallinn |Hà Nội :
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Tel Aviv | Kfar Saba | Netanya | Be'Er Sheva | Yavne |Remote :
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Kyiv |Lima Region :
Lima |France :
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Niš |Bohemia :
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