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 Clinical Study Manager II at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.
What You Will Do:
You will manage day-to-day clinical trial management activities, supporting your team to deliver quality outcomes.
Key responsibilities include:
- Lead the planning, execution, and monitoring of complex clinical trials, ensuring adherence to regulatory requirements and project timelines.
- Collaborate closely with cross-functional teams, including investigators, vendors, and internal stakeholders, to drive the successful implementation of advanced clinical studies.
- Develop and manage comprehensive study plans, budgets, and timelines, optimizing resource utilization and maintaining a focus on efficiency.
- Spearhead the resolution of intricate issues and challenges that may arise during clinical trials, employing strategic problem-solving skills and effective communication strategies.
- Implement and oversee robust monitoring and validation processes throughout the study lifecycle, ensuring data integrity and maintaining high-quality standards.
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:
- Bachelor's degree in a relevant scientific discipline or healthcare-related field
- experience in Biosample operations, biomarker programs, and sample lifecycle management
- Central laboratory operations
- Extensive experience in clinical study management, showcasing a good grasp of the drug development process and regulatory landscape.
- Proven ability in project management, handling multiple tasks concurrently, and effectively prioritizing duties.
- Exceptional communication and interpersonal skills, fostering effective collaboration with diverse cross-functional teams and external partners.
- Detail-oriented with an unwavering dedication to data accuracy and maintaining the highest quality standards in advanced clinical trials.
- #LI-OB1
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
Skills Required
- Bachelor's degree in a relevant scientific discipline or healthcare-related field
- Experience in biosample operations, biomarker programs, and sample lifecycle management
- Central laboratory operations experience
- Extensive experience in clinical study management and knowledge of drug development and regulatory landscape
- Proven project management ability, handling multiple tasks and prioritizing duties
- Exceptional communication and interpersonal skills for cross-functional collaboration
- Detail-oriented with dedication to data accuracy and high quality standards
ICON plc Compensation & Benefits Highlights
The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about ICON plc and has not been reviewed or approved by ICON plc.
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Healthcare Strength — Benefits are described as comprehensive, with medical coverage and wellness initiatives highlighted. Larger sites are also associated with added wellness supports such as onsite fitness options and access to an employee assistance program.
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Leave & Time Off Breadth — Time-off and flexibility provisions are positioned as a meaningful part of the total package, including vacation/annual leave and flexible work scheduling. Flexibility is sometimes cited as helping offset long hours in certain roles.
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Retirement Support — Retirement and savings support is presented as a core component of the benefits package, including offerings such as pension arrangements in some locations and a U.S. 401(k) plan with company match. Financial planning resources are also emphasized as part of broader security benefits.
ICON plc Insights
What We Do
Since our foundation in Dublin, Ireland in 1990, our mission has been to help our clients to accelerate the development of drugs and devices that save lives and improve quality of life. We do this by delivering best in class information, solutions and performance, with an unyielding focus on quality at all times. We offer a full range of consulting, development and commercialisation services from a global network of offices in 53 countries. We focus our innovation on the factors that are critical to our clients – reducing time to market, reducing cost, and increasing quality – and our global team of experts has extensive experience in a broad range of therapeutic areas.
