Supervisor, Pharmacovigilance

ICON plc

Supervisor, Pharmacovigilance overseeing safety monitoring and reporting for clinical trials at ICON healthcare. Collaborating with teams to ensure compliance with pharmacovigilance regulations.

Posted 7/10/2026full-timeSofia • 🇧🇬 BulgariaSeniorLeadWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates extensive experience in pharmacovigilance and drug safety, with a strong focus on compliance with global regulations and effective team management. Proven ability to lead safety reporting operations and collaborate with cross-functional teams to optimize processes.

Highest-signal resume keywords

PharmacovigilanceDrug SafetyGlobal Regulatory ComplianceTeam ManagementSafety Reporting

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

PharmacovigilanceDrug SafetySafety ReportingClinical TrialsPost-Marketing SurveillanceRegulatory SubmissionsSafety Submissions WorkflowDetail OrientationAccuracy Management

Soft Skills

LeadershipCommunicationOrganizational SkillsCollaborationTeam Management

Industry Keywords

Global Pharmacovigilance RegulationsStandard Operating ProceduresCross-Functional CollaborationSafety Reporting Best Practices

About the role

Key responsibilities & impact

Supervising the day-to-day pharmacovigilance safety reporting operations, ensuring timely and accurate reporting to regulatory authorities
Collaborating with cross-functional teams, including clinical operations and regulatory affairs, to optimize pharmacovigilance processes
Ensuring compliance with global regulatory requirements and internal standard operating procedures for safety reporting
Managing safety submissions workflow and submission to regulatory authorities
Providing leadership and training to the pharmacovigilance team, ensuring adherence to best practices in safety reporting.

Requirements

What you’ll need

8+ years in pharmacovigilance or drug safety
Bachelor’s degree in life sciences, pharmacy, or a related field
Team Management skills
Solid experience in pharmacovigilance or drug safety, with a focus on clinical trials or post-marketing surveillance
Strong knowledge of global pharmacovigilance regulations and guidelines
Excellent communication, leadership, and organizational skills, with the ability to manage a team effectively
Detail-oriented with the ability to manage multiple tasks and ensure accuracy in safety reporting.

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