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Clinical Research Associate II / Senior Clinical Research Associate
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What they do
A Clinical Research Associate is responsible for running clinical trials, usually for an organization undertaking pharmacological drug testing. Will ensure that trials adhere to good clinical practice guidelines for monitoring clinical trials.
$105,028 / year median in the U.S.
+1% projected growth
Job Description
North America | Remote | Sponsor-Dedicated ( FSP ) Opportunities ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. 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. About the Opportunity 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. Depending on your experience level, you may:
+ 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) What We're Looking For CRA II
+ 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 Senior CRA
+ 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
+ Experience mentoring or supporting other CRAs is advantageous For all applicants
+ Strong communication and relationship-building skills
+ Willingness to travel as required
+ Passion for advancing clinical research and improving patient outcomes When you join ICON Strategic Solutions, you gain the best of both worlds:
+ Work within dedicated sponsor environments
+ Build expertise with leading global pharmaceutical and biotechnology companies
+ A To view full details and how to apply, please login or create a Job Seeker account