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ICON plc

Manager, Pharmacovigilance

ICON plc

. Oversee pharmacovigilance activities, ensuring the safety and efficacy of clinical trial products throughout their lifecycle .

Posted 11/5/2026full-timeChennai • IndiaMid-LevelSeniorWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in pharmacovigilance and drug safety management, ensuring compliance with regulatory guidelines and internal standards while leading teams in safety data evaluation and reporting. Strong analytical and leadership skills are essential for managing multiple projects and collaborating with cross-functional teams.

Highest-signal resume keywords
Pharmacovigilance ManagementRegulatory ComplianceSafety Data AnalysisTeam LeadershipCross-Functional Collaboration

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills
PharmacovigilanceDrug Safety ManagementSafety Reporting StandardsRisk AssessmentSafety Data Evaluation
Soft Skills
LeadershipOrganizational SkillsCommunication SkillsInterpersonal SkillsDetail-Oriented
Industry Keywords
Clinical TrialsRegulatory GuidelinesQuality AssuranceAdverse Events ReportingSafety Assessments

About the role

Key responsibilities & impact
  • Oversee pharmacovigilance activities, ensuring the safety and efficacy of clinical trial products throughout their lifecycle
  • Coordinate pharmacovigilance and drug safety delivery
  • Resolve issues and develop team capability
  • Lead the pharmacovigilance team in collecting, evaluating, and reporting adverse events
  • Ensure compliance with regulatory guidelines and internal standards
  • Develop and implement pharmacovigilance processes and policies
  • Collaborate with clinical, regulatory, and quality assurance teams on safety assessments and timely safety-data reporting
  • Provide training and guidance on pharmacovigilance regulations, practices, and procedures
  • Monitor and analyze safety-data trends
  • Prepare risk assessments and present findings to relevant stakeholders
  • Ensure pharmacovigilance activities comply with global regulatory requirements and internal quality standards

Requirements

What you’ll need
  • Bachelor's degree in life sciences, pharmacy, or a related field is preferred, with extensive experience in pharmacovigilance or drug safety management
  • Proven experience in managing pharmacovigilance teams and activities
  • Thorough understanding of regulatory requirements and safety reporting standards
  • Strong analytical skills, with experience in assessing safety data and preparing safety reports for regulatory submission
  • Excellent leadership and organizational skills
  • Ability to manage multiple projects and deliver results in a fast-paced environment
  • Exceptional communication and interpersonal skills
  • Ability to collaborate effectively with cross-functional teams and external stakeholders
  • Detail-oriented, proactive, and committed to maintaining the highest standards of safety and quality in pharmacovigilance operations
  • Willingness to travel as required (approximately 15%)
  • Legal right to work in the country where the role is based

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