Clinical Trial Manager
ICON plc
Summary
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.
Job description
As a Clinical Trial Manager at ICON, you will manage clinical trial operations activities, supporting your team and stakeholders to deliver high-quality outcomes across our clinical programmes.
What You Will Do
You will manage day-to-day clinical trial management activities, supporting your team to deliver quality outcomes. Key responsibilities include:
- Plan and manage all aspects of clinical trials, ensuring adherence to timelines, budget, and quality standards.
- Collaborate with cross-functional teams to establish and implement clinical trial protocols and procedures.
- Build and manage strong relationships with trial investigators and stakeholders.
- Ensure all trials are conducted in compliance with local, national, and international regulations and ethical guidelines.
- Problem-solve and make critical decisions regarding trial design, vendor selection, and risk management.
Your Profile
You will have solid clinical trial management experience, with the ability to manage competing priorities and develop your team. Required qualifications and experience:
- University degree in medicine, science, or equivalent combination of education & experience.
- A minimum of three years of industry clinical trial management experience
- Demonstrated ability to drive the clinical deliverables of a study
- Experience managing phase I (healthy volunteer) studies
- Some travel may be required
Requirements
- University degree in medicine, science, or equivalent combination of education & experience.
- A minimum of three years of industry clinical trial management experience
- Demonstrated ability to drive the clinical deliverables of a study
- Experience managing phase I (healthy volunteer) studies
- Some travel may be required
Benefits
- Competitive Base Salary
- Performance-Related Incentives
- Medical, Dental & Vision
- Retirement and Pension Plans
- Life Assurance
- Disability Coverage
- Employee Assistance Programs
- 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.