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 Senior Manager, Clinical Operations at ICON, you will be critical in overseeing the operational aspects of clinical trials to ensure their successful execution.

What You Will Do:

You will manage clinical operations activities across your area, ensuring your team delivers to the highest standards.

Key responsibilities include:

• Leading and managing clinical operations teams to ensure the effective planning, execution, and monitoring of clinical trials.
• Developing and implementing strategies to streamline clinical trial processes, enhance operational efficiency, and ensure adherence to project timelines and budgets.
• Collaborating with cross-functional teams, including clinical research, data management, and regulatory affairs, to ensure alignment and integration of clinical operations with overall project goals.
• Overseeing site management activities, including site selection, initiation, monitoring, and closeout, to ensure high-quality data and compliance with study protocols.
• Monitoring trial performance metrics, identifying areas for improvement, and implementing corrective actions to address any issues and optimize trial outcomes.

Your Profile:

You will have a strong background in clinical operations, with proven management experience and a commitment to quality delivery.

Required qualifications and experience:

• Degree in Life Sciences, Clinical Research, or a related field.
• Extensive experience in clinical operations, with a proven track record of managing and executing clinical trials across various phases and therapeutic areas.
• Strong leadership and team management skills, with the ability to guide and develop a team of clinical operations professionals.
• In-depth knowledge of clinical trial regulations, Good Clinical Practice (GCP), and industry standards, with experience in optimizing trial processes and managing operational challenges.
• Excellent organizational and communication skills, with the capability to effectively collaborate with internal teams and external partners to achieve project objectives.
• Willingness to travel as required (approximately 30%)

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