Pharmacovigilance Specialist – Drug Safety Role

About the role

ICON is seeking a Pharmacovigilance Specialist to join its global drug safety team. You will be responsible for monitoring the safety of pharmaceutical products, analysing adverse event data, and ensuring compliance with regulatory requirements.

Key responsibilities

• Collect, review, and analyse adverse event reports to guarantee timely and accurate regulatory reporting.
• Conduct risk assessments and signal detection activities to identify potential safety concerns.
• Collaborate with cross‑functional teams to address safety‑related inquiries and investigations.
• Prepare and submit safety reports and regulatory submissions within required timelines.
• Stay up‑to‑date with pharmacovigilance regulations and industry best practices.

Required profile

• Bachelor's degree in a scientific or healthcare‑related discipline.
• Experience in pharmacovigilance, drug safety, or a related field, preferably in a clinical or pharmaceutical environment.
• Strong analytical abilities and meticulous attention to detail.
• Excellent communication and interpersonal skills for effective teamwork.
• Commitment to high standards of quality and regulatory compliance.
• Willingness to travel up to 15% as needed.

Required skills

What we offer

• Competitive base salary and performance‑related incentives.
• Health, dental and vision coverage, retirement and pension plans.
• Life assurance, disability coverage, and employee assistance programmes.
• Learning and development opportunities through structured training and career pathways.