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 values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.

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.

What You Will Do:

You will take responsibility for pharmacovigilance and drug safety deliverables, applying your skills to ensure quality and efficiency.

Key responsibilities include:

• 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:

You will bring relevant pharmacovigilance and drug safety experience, along with the following qualifications and skills.

Required qualifications and experience:

• Bachelor's degree in a relevant scientific discipline or healthcare-related field
• At least 3 years of experience in pharmacovigilance, drug safety, or a related area, preferably within a clinical or pharmaceutical setting.
• Hands-on experience in handling pharmacovigilance (PV) cases from clinical trials, including case processing, assessment, and follow-up.
• Proven ability to lead PV projects, effectively resolve issues, manage cross-functional stakeholders, and present insights and updates to sponsors.
• 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.
• Must be amenable to work in hybrid set-up (2-3x a week in office at Makati City)

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.

Benefits may include:

• 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

Benefits may vary depending on role and location.

Visit our careers site to read more about the benefits ICON offers.

Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.

If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.

Are you a current ICON Employee? Please click here to apply