About The Position
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. At ICON Strategic Solutions, we're continually growing our network of talented Clinical Research Associates across North America. As we expand our partnerships with leading global sponsors, we are seeking experienced CRA II and Senior CRA professionals interested in sponsor-dedicated opportunities. As a Clinical Research Associate within our sponsor-dedicated environment, you will play a critical role in the successful delivery of clinical trials, helping bring innovative therapies to patients worldwide.
Requirements
- Bachelor's degree in a scientific, healthcare, or related field
- Clinical monitoring experience within the pharmaceutical, biotech, or CRO industry
- Strong knowledge of ICH-GCP, clinical trial regulations, and monitoring practices
- Ability to work independently while collaborating effectively across teams
- Significant clinical monitoring experience across multiple studies and sites
- Advanced knowledge of clinical trial processes, regulations, and site management
- Proven ability to manage priorities and drive study quality independently
- Strong communication and relationship-building skills
- Willingness to travel as required
- Passion for advancing clinical research and improving patient outcomes
- Having the legal right to work in the country where the role is based.
Nice To Haves
- Experience mentoring or supporting other CRAs is advantageous
Responsibilities
- Conduct site qualification, initiation, routine monitoring, and close-out visits
- Ensure protocol compliance, patient safety, data quality, and regulatory adherence
- Build strong relationships with investigative sites and key stakeholders
- Identify and proactively resolve site and study issues
- Collaborate with cross-functional teams to support successful study delivery
- Support inspection readiness and high-quality study execution
- Mentor and guide less experienced CRAs (Senior CRA level)
Benefits
- 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
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
