About this role
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 Sr. CRA at ICON, you will oversee and manage clinical trial sites, ensuring that studies are conducted in accordance with regulatory requirements, study protocols, and company standards.
What You Will Do:
Your focus will be on coordinating clinical trial monitoring delivery, resolving issues, and developing team capability.
Key responsibilities include:
Leading site management activities, including site selection, initiation, monitoring, and close-out visits, to ensure compliance with study protocols and regulatory guidelines.
Serving as the primary point of contact for clinical sites, addressing site queries, and resolving issues to maintain site engagement and performance.
Ensuring the integrity of clinical data by conducting thorough source data verification, reviewing site records, and monitoring for protocol deviations.
Mentoring and providing guidance to CRAs, contributing to their professional development and supporting the consistent application of best practices across studies.
Collaborating with cross-functional teams, including clinical project managers, data managers, and biostatisticians, to ensure the successful execution of clinical trials.
Your Profile:
You will have solid clinical trial monitoring 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
Fluent in English and French, with strong verbal and written communication skills.
Extensive experience as a Clinical Research Associate within the pharmaceutical, biotech, or CRO industry, with a proven track record of managing complex clinical trials.
In-depth knowledge of ICH-GCP guidelines, regulatory requirements, and clinical trial processes.
Strong leadership and mentoring skills, with the ability to manage and motivate CRAs and site staff effectively.
Excellent communication, organizational, and problem-solving skills, with a proactive approach to managing site performance and resolving issues.
Willingness to travel as required (approximately 60%)
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
About ICON plc
Global contract research organization providing outsourced clinical development services. Headquartered in Dublin, Ireland.
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