PV Specialist

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

As a Pharmacovigilance Specialist at ICON, you will be responsible for monitoring the safety of pharmaceutical products by analyzing, interpreting, and reporting adverse event data in accordance with regulatory requirements.

Responsibilities

• Collecting, reviewing, and analyzing adverse event reports to ensure timely and accurate reporting in compliance with regulatory guidelines.
• Conducting risk assessments and signal detection activities to identify and evaluate potential safety concerns.
• Collaborating with cross-functional teams to support safety-related inquiries and investigations.
• Preparing and submitting safety reports and regulatory submissions in a timely manner.
• Staying current on pharmacovigilance regulations and industry best practices to enhance the safety framework.

Your Profile

• Bachelor's degree in a relevant scientific discipline or healthcare-related field
• Experience in pharmacovigilance, drug safety, or a related area, preferably within a clinical or pharmaceutical setting.
• Strong analytical skills and attention to detail in data collection and reporting.
• Excellent communication and interpersonal skills, enabling effective collaboration with diverse teams.
• A commitment to upholding high standards of quality and compliance in all pharmacovigilance activities.
• Willingness to travel as required (approximately 15%)

Rewards & Benefits

• 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