Analytical Monitor

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 Central Review Lead at ICON, you will oversee and coordinate centralized review activities for clinical trials, contributing to the advancement of innovative treatments and therapies.

What You Will Do:

You will oversee clinical research workstreams, ensuring deliverables meet quality and timeline expectations.

Key responsibilities include:

• Lead and oversee the planning, execution, and monitoring of centralized review activities, including imaging assessments, laboratory analyses, and other centralized evaluations.
• Collaborate closely with study teams, clinical sites, and external vendors to ensure the timely and accurate collection, transfer, and interpretation of clinical trial data.
• Develop and implement standardized processes, protocols, and quality control measures to optimize the efficiency, accuracy, and reliability of centralized review operations.
• Provide leadership and guidance to central review teams, ensuring adherence to protocol requirements, regulatory standards, and best practices.
• Proactively identify and address issues, deviations, and risks related to central review activities, driving continuous improvement and operational excellence.

Your Profile:

You will have solid clinical research experience, with the ability to manage competing priorities and develop your team.

Required qualifications and experience:

• Bachelor's degree in life sciences, computer science, or a related discipline
• Extensive experience in clinical research, data management, or study coordination within the pharmaceutical, biotechnology, or CRO industry.
• Strong leadership and project management skills with a track record of successfully leading cross-functional teams and managing complex projects.
• In-depth knowledge of central review methodologies, technologies, and regulatory requirements (e.g., ICH GCP, FDA regulations).
• Excellent communication, interpersonal, and problem-solving abilities, with the ability to effectively collaborate and communicate with stakeholders at all levels.

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