Pharmacovigilance Project Manager

Description du poste:

JR151203

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 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.

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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