Manager, Clinical Operations
ICON plc
Summary
As a Manager, Clinical Operations at ICON, you will oversee the execution of clinical trials, ensuring that they are conducted efficiently, on time, and in compliance with regulatory requirements.
Job description
What You Will Do
Your focus will be on coordinating clinical operations delivery, resolving issues, and developing team capability. Key responsibilities include:
- Leading the operational planning and execution of clinical trials, ensuring adherence to protocols and timelines.
- Engaging with cross-functional teams to optimize trial design and enhance operational efficiency throughout the clinical development process.
- Monitoring trial progress and performance metrics, providing insights to inform decision-making and drive continuous improvement.
- Mentoring and developing junior staff, fostering a culture of collaboration and excellence within the team.
- Building strong relationships with internal and external stakeholders to facilitate smooth communication across clinical operations.
Your Profile
You will have solid clinical operations 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
- Experience in managing clinical teams, with a solid understanding of Clinical Research Associate requirements
- Clinical Research Associate experience required
- Strong leadership skills with the ability to motivate teams effectively in a dynamic environment.
- Proficiency in project management tools and methodologies, with a keen focus on optimizing processes.
- Excellent communication and interpersonal skills, with a proven ability to influence stakeholders and drive successful outcomes.
- Willingness to travel as required (approximately 30%)
Requirements
- Bachelor's degree in a relevant scientific discipline or healthcare-related field
- Experience in managing clinical teams, with a solid understanding of Clinical Research Associate requirements
- Clinical Research Associate experience required
- Strong leadership skills with the ability to motivate teams effectively in a dynamic environment.
- Proficiency in project management tools and methodologies, with a keen focus on optimizing processes.
- Excellent communication and interpersonal skills, with a proven ability to influence stakeholders and drive successful outcomes.
- Willingness to travel as required (approximately 30%)
Benefits
- Competitive base salary
- Performance related incentives
- Medical, Dental & Vision
- Retirement and pension plans
- Life assurance and disability coverage
- Employee assistance programmes
- Wellbeing resources
- Learning and development opportunities
Company overview
ICON plc is a global leader in clinical research and healthcare intelligence, founded in Dublin, Ireland in 1990. As one of the world's largest contract research organizations (CROs), ICON provides comprehensive outsourced development services to pharmaceutical, biotechnology, and medical device companies worldwide. The company operates in 55 countries with approximately 41,900 employees, offering end-to-end solutions that span the entire product development lifecycle. ICON's service portfolio includes clinical research services, adaptive trials, biosimilars, commercialization and outcomes consulting, medical imaging, laboratory services, and strategic support for traditional and digital health technologies. The company specializes in therapeutic areas such as oncology, cardiovascular diseases, central nervous system disorders, rare diseases, and women's health. With its 2021 acquisition of PRA Health Sciences, ICON significantly expanded its capabilities and market position, becoming a dominant force in the global CRO industry. The company is publicly traded on NASDAQ under the ticker ICLR and reported $8.28 billion in revenue for 2024.