Pharmacovigilance Project Manager

ICON Clinical Research; Ciudad de México; Hybrid; MXN 600,000 - 900,000; Full time

Benefits offered by this job

Annual leave

Health insurance

Retirement planning

Employee assistance program

Life insurance

Flexible benefits

Job summary

ICON Clinical Research is seeking a Pharmacovigilance Project Manager for a home-based role in CDMX, Mexico. You will lead pharmacovigilance activities across trials and post-marketing studies, coordinating with clinical, regulatory, and data management teams.

The ideal candidate has extensive PV/drug safety experience, strong project management skills, and the ability to mentor teams while ensuring regulatory compliance and timely safety reporting.

Qualifications

• Bachelor's degree in a relevant scientific discipline or healthcare-related field.
• Extensive experience in pharmacovigilance or drug safety with regulatory knowledge.
• Proven project management skills leading complex PV projects and cross-functional teams.
• Excellent organizational and analytical abilities to manage detailed project plans.
• Strong communication and interpersonal skills to collaborate with diverse stakeholders.

Responsibilities

• Coordinate pharmacovigilance and drug safety delivery across trials and post-marketing studies.
• Develop and implement project plans with timelines and budgets.
• Coordinate cross-functional teams for safety monitoring activities.
• Oversee collection, evaluation, and reporting of adverse events to authorities.
• Provide strategic guidance and mentor PV staff to improve performance.
• Monitor progress, identify risks, and implement mitigation.

Skills

Pharmacovigilance experience

Drug safety

Project management

Cross-functional collaboration

Regulatory knowledge

Communication skills

Education

Bachelor's degree in a relevant scientific discipline or healthcare-related field

Job description

Home Based - CDMX

At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise.

As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.

As a Pharmacovigilance Project Manager at ICON, you will be responsible for leading and oversee pharmacovigilance activities across clinical trials and post-marketing studies.

What You Will Do:

Your focus will be on coordinating pharmacovigilance and drug safety delivery, resolving issues, and developing team capability.

Key responsibilities include:

• Managing all aspects of pharmacovigilance projects, including planning, execution, and delivery, while ensuring adherence to regulatory requirements and company standards.

• Developing and implementing project plans, including timelines, budgets, and resource allocation, to meet project goals and milestones.

• Coordinating with cross-functional teams, including clinical, regulatory, and data management, to ensure the successful integration and execution of safety monitoring activities.

• Overseeing the collection, evaluation, and reporting of adverse events, and ensuring timely and accurate submission to regulatory authorities and sponsors.

• Providing strategic guidance and leadership to pharmacovigilance teams, including mentoring and training staff to enhance project performance and compliance.

• Monitoring project progress, identifying risks, and implementing mitigation strategies to address any issues that may impact project success.

Your Profile:

You will have solid pharmacovigilance and drug safety experience, with the ability to manage competing priorities and develop your team.

Required qualifications and experience:

• Bachelor's degree in a relevant scientific discipline or healthcare-related field

• Extensive experience in pharmacovigilance or drug safety, with a strong understanding of safety reporting and regulatory requirements.

• Proven project management skills, with experience leading complex pharmacovigilance projects and managing cross-functional teams.

• Excellent organizational and analytical skills, with the ability to develop and execute detailed project plans and manage multiple priorities.

• Strong communication and interpersonal skills, with the ability to collaborate effectively with diverse stakeholders and drive project success.

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)