ICON plc
Senior Clinical Trial Associate
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Senior Clinical Trial Associate – Cambridge (England)
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.
About the Role
As a Senior Clinical Trial Associate at ICON Plc, you will support the management and execution of clinical trials by handling a range of administrative and operational tasks while working autonomously and leading project deliverables with impact.
What You Will Do
You will take ownership of clinical trial management deliverables, applying your expertise to complex challenges.
Key Responsibilities:
- Provide administrative support for clinical trials, including:
- Managing documentation
- Coordinating meetings
- Maintaining trial-related records
- Assist in the preparation and submission of regulatory documents, ensuring compliance with study protocols and regulatory requirements
- Collaborate with cross-functional teams to support trial operations and proactively resolve issues during study execution
- Monitor and track trial progress, including:
- Managing site communications
- Ensuring timely delivery of study materials
- Build and maintain strong relationships with site staff and other stakeholders to facilitate smooth trial operations and support project success
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Your Profile
You will have a strong foundation in clinical trial management, with the ability to work independently and guide junior colleagues. ICON is seeking a motivated professional with:
Required Qualifications & Experience:
- Bachelor’s degree in a relevant scientific discipline (e.g., pharmacology, medicine, life sciences) or healthcare-related field
- Extensive experience in clinical trial support, with in-depth knowledge of:
- Clinical trial processes
- Regulatory requirements (e.g., ICH-GCP, FDA/EMA guidelines)
- Strong organisational and multitasking skills to manage multiple projects and deadlines effectively
- Proficient in clinical trial management systems (e.g., StudyKit, Central, Veeva) and relevant software (e.g., Excel, project management tools)
- Exceptional communication and interpersonal skills, with the ability to collaborate across global teams
- Problem-solving aptitude to resolve operational challenges autonomously
Employment Eligibility:
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 growth. Benefits may include:
- Base salary + performance-related incentives
- Health and wellbeing programmes:
- Medical, dental, and vision coverage (location-dependent)
- Life assurance and disability cover
- Retirement and pension plans
- Employee assistance programmes and wellbeing resources
- Learning and development opportunities, including:
- Structured training programmes
- Career progression pathways
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Benefits may vary depending on role and location. Visit our careers site for detailed information.
Inclusion & Accessibility
ICON is an equal opportunity employer and is committed to building an inclusive and accessible workplace where everyone feels valued. If you require reasonable accommodations during the recruitment process, please contact us here with your needs.
Why Join ICON?
You will be part of a world-class clinical research organisation dedicated to delivering innovative medicines and medical devices that transform patient lives.
- Make a meaningful impact by contributing to pioneering research
- Join a diverse, global team committed to sustainability and community engagement
- Thriving work culture of collaboration, agility, and inclusion
- Work alongside some of the brightest and most talented professionals in the healthcare sector
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