Senior Pharmacovigilance Associate

ICON plc

. Lead the collection, evaluation, and processing of adverse event reports in accordance with regulatory guidelines and company policies .

Posted 9/24/2026full-timeRemote • ChileSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in pharmacovigilance processes, including adverse event reporting and signal detection, while effectively managing data analysis and regulatory compliance. Strong communication and mentorship abilities enhance collaboration across medical and clinical teams.

Highest-signal resume keywords

PharmacovigilanceAdverse Event ReportingData AnalysisRegulatory ComplianceSignal Detection

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Applicant Tracking System Keywords

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Hard Skills

Data InterpretationPharmacovigilance Process ManagementRegulatory Document PreparationTrend IdentificationDatabase Maintenance

Soft Skills

Analytical ThinkingInterpersonal SkillsCommunication SkillsMentorshipCollaboration

Tools & Technologies

Pharmacovigilance DatabasesData Management SystemsMicrosoft Office Suite

Industry Keywords

Regulatory GuidelinesSafety DataRisk ManagementClinical RelevanceRegulatory Audits

About the role

Key responsibilities & impact

Lead the collection, evaluation, and processing of adverse event reports in accordance with regulatory guidelines and company policies
Conduct data analysis and interpretation of safety data, identifying trends and potential safety signals
Prepare and submit periodic safety update reports (PSURs) and other regulatory documents
Collaborate with medical and clinical teams to assess the clinical relevance of adverse events and contribute to risk management activities
Oversee the maintenance and integrity of pharmacovigilance databases
Provide training and mentorship to junior team members
Engage in regulatory audits and inspections, ensuring readiness and compliance

Requirements

What you’ll need

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
Excellent communication and interpersonal skills, with the ability to work collaboratively across cross-functional teams
Proficiency in pharmacovigilance databases and data management systems, as well as Microsoft Office Suite
Ability to work independently and manage multiple priorities in a fast-paced environment
Willingness to travel as required (approximately 15%)
Legal right to work in Chile

Benefits

Comp & perks

Competitive base salary and performance related incentives
Health and wellbeing programmes including medical, dental, and vision coverage where applicable
Retirement and pension plans
Life assurance and disability coverage
Employee assistance programmes and wellbeing resources
Learning and development opportunities through structured training and career pathways