Clinical Study Manager
ICON plc
Summary
As a Clinical Study Manager at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.
Job description
What You Will Do
Your focus will be on coordinating clinical trial management delivery, resolving issues, and developing team capability.
- Oversee the planning, execution, and monitoring of clinical trials to ensure compliance with regulatory requirements and project timelines.
- Collaborate with cross-functional teams, including investigators, vendors, and internal stakeholders, to drive the successful implementation of clinical studies.
- Develop and manage study budgets, resources, and timelines, ensuring efficient use of resources and adherence to study plans.
- Lead the resolution of issues and challenges that may arise during clinical trials, employing effective problem-solving skills and communication strategies.
- Ensure data integrity and quality by implementing rigorous monitoring and validation processes throughout the study lifecycle.
Your Profile
You will have solid clinical trial management experience, with the ability to manage competing priorities and develop your team.
- Bachelor's degree in a relevant scientific discipline or healthcare-related field
- Proven experience in clinical study management, with a strong understanding of the drug development process and regulatory requirements.
- Excellent project management skills, including the ability to handle multiple tasks simultaneously and prioritize effectively.
- Strong communication and interpersonal skills, with the ability to collaborate effectively with cross-functional teams and external partners.
- Detail-oriented with a focus on ensuring data accuracy and maintaining high-quality standards in clinical trials.
Requirements
- Bachelor's degree in a relevant scientific discipline or healthcare-related field
- Proven experience in clinical study management
- Strong understanding of the drug development process and regulatory requirements
- Excellent project management skills
- Ability to handle multiple tasks simultaneously and prioritize effectively
- Strong communication and interpersonal skills
- Ability to collaborate effectively with cross-functional teams and external partners
- Detail-oriented with a focus on ensuring data accuracy and maintaining high-quality standards in clinical trials
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.