Pharmacovigilance Associate

ICON Clinical Research; Manila; Hybrid; PHP 600,000 - 900,000; Full time

Job summary

ICON Clinical Research is hiring a Pharmacovigilance Associate in the Philippines with a hybrid work arrangement. You will monitor drug safety, review adverse event reports, and support regulatory submissions in a collaborative, compliant environment. A degree in a relevant field and PV experience are required.

You will work with a global team to ensure high standards of safety data collection, analysis, and reporting, contributing to patient safety and regulatory compliance.

Qualifications

• Bachelor's degree in a scientific or healthcare-related field, required.
• Minimum 2 years' experience in pharmacovigilance or drug safety.
• Strong analytical skills with precise data collection and reporting.
• Excellent communication and interpersonal abilities for teamwork.
• Commitment to high quality, regulatory compliance in PV activities.
• Willingness to work in a hybrid setup: 2–3 days in Makati City.

Responsibilities

• Collecting and reviewing adverse event reports for timely regulatory reporting.
• Performing signal detection and risk assessments to identify safety issues.
• Collaborating with cross-functional teams on safety inquiries and investigations.
• Keeping up-to-date with pharmacovigilance regulations and best practices.
• Assisting in preparing safety reports and regulatory submissions.

Skills

Pharmacovigilance

Data analysis

Communication

Attention to detail

Collaboration

Compliance

Education

Bachelor's degree in a relevant scientific discipline

Job description

PV Associate - Philippines - Hybrid

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 Associate at ICON, you will monitor and ensure the safety of pharmaceutical products by collecting, analyzing, and reporting adverse event information.

What You Will Do:

Your role will involve delivering pharmacovigilance and drug safety work to a high standard, working closely with your team and stakeholders.

Key responsibilities include:

• Collecting and reviewing adverse event reports to ensure accurate and timely reporting in accordance with regulatory guidelines.

• Conducting signal detection and risk assessment activities to identify potential safety issues.

• Collaborating with cross-functional teams to support safety-related inquiries and investigations.

• Maintaining up-to-date knowledge of pharmacovigilance regulations and industry best practices.

• Assisting in the preparation of safety reports and regulatory submissions.

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 2 years of experience in pharmacovigilance, drug safety, or a related area, preferably within a clinical or pharmaceutical environment.

• Strong analytical skills with attention to detail in data collection and reporting.

• Excellent communication and interpersonal skills, enabling effective collaboration with team members and stakeholders.

• A commitment to maintaining high standards of quality and compliance in all pharmacovigilance activities.

• Willingness to work in a hybrid setup (2-3x a week RTO in Makati City)

What ICON can offer you:

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our benefits examples include:

• Various annual leave entitlements

• A range of health insurance offerings to suit you and your family’s needs.

• Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.

• Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being.

• Life assurance

• Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.

Visit our careers site (https://careers.iconplc.com/benefits) to read more about the benefits ICON offers.

At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here (https://careers.iconplc.com/reasonable-accommodations)