Remote Clinical Research Associate Job at ICON, USA | Life Sciences | Apply Now
If you are an experienced on-site monitor or a qualified Registered Nurse (RN) looking to advance your career with a global healthcare intelligence leader, this full-time role at ICON plc is an exceptional career move. Offered as a remote, home-based position in Utah, this role places you on the front lines of clinical trial delivery and patient data integrity. For detail-oriented monitoring professionals searching for a high-impact Clinical Research Associate Job, this position within ICON’s Functional Service Provider (FSP) division offers direct ownership of the full clinical site lifecycle—from selection to close-out. It serves as an elite launchpad to advance a long-term ICON career and stands out as a premier choice for anyone tracking a competitive Life Sciences Job with strong regional travel efficiency.
About The Company
ICON plc is a world-leading global Contract Research Organization (CRO) and healthcare intelligence powerhouse driven by a unified mission to accelerate the development of innovative medicines, medical devices, and diagnostic tools. Managing multi-center operations across the globe, ICON provides the underlying regulatory, clinical, and data infrastructure that helps pharmaceutical innovators combat global diseases. This specific vacancy sits within ICON Strategic Solutions, operating under a highly collaborative Functional Service Provider (FSP) model. In this setup, you are embedded directly into a single, major global pharmaceutical sponsor’s internal study infrastructure. This architecture allows you to focus exclusively on that sponsor’s specific pipeline protocols, proprietary clinical technologies, and data monitoring systems, all while simultaneously enjoying the job security, international network, and comprehensive employee benefits provided by ICON.
Clinical Research Associate Job – Key Responsibilities
The Clinical Research Associate (CRA) acts as the primary point of contact between investigational sites and the sponsor, ensuring clinical trials are conducted, recorded, and reported in strict compliance with quality guidelines.
Your core site management, document auditing, and milestone verification duties include:
- Full Site Lifecycle Audits: Conducting all types of site visits, including Site Selection Visits (SSV), Site Initiation Visits (SIV), routine Interim Monitoring Visits (IMV), and formal Close-Out Visits (COV).
- Regulatory Compliance Oversight: Verifying site compliance with international ICH-GCP frameworks, active Standard Operating Procedures (SOPs), and local FDA regulations to advance this Clinical Research Associate Job.
- Systems & Documentation Curation: Maintaining real-time, up-to-date site statuses, metrics, and documentation logs within Clinical Trial Management Systems (CTMS) and electronic Trial Master File (eTMF) architectures.
- Safety & Deviation Triage: Monitoring patient safety parameters closely, ensuring the rapid and accurate reporting of Adverse Events (AEs), Serious Adverse Events (SAEs), and Product Quality Complaints (PQCs).
- Investigational Product Accountability: Overseeing strict drug accountability pipelines, ensuring the proper storage conditions, chain of custody, return, or witnessed destruction of study supplies.
- Data Query Resolution: Reviewing electronic case report forms (eCRFs) against source documents, resolving data queries, and driving timely, high-quality data entry at the site level to support this Life Sciences Job.
- Site Staff Training Support: Tracking site staff credentials, verifying required training logs, and ensuring that clinical facilities remain inspection-ready at all times.
Qualifications & Profile Requirements For Clinical Research Associate Job
ICON seeks a systematic, detail-oriented clinical research professional who demonstrates strong problem-solving habits and the communication skills required to manage multiple site priorities.
- Required Academic & Legal Criteria:
- Educational Foundation: A completed Bachelor’s degree in the Life Sciences (or equivalent natural science field), or a formal, active qualification as a Registered Nurse (RN).
- Work Authorization: Must possess valid authorization to work in the United States indefinitely without current or future corporate visa sponsorship to secure an ICON career.
- Essential Knowledge & Experience:
- Industry Track Record: A minimum of 2+ years of independent, on-site clinical monitoring experience executed within the pharmaceutical or CRO industry sectors.
- Therapeutic Breadth: Demonstrated experience monitoring clinical trials across multiple therapeutic areas.
- Clinical Systems Fluency: Strong, practical proficiency navigating international ICH-GCP guidelines, local regulatory requirements, and standard clinical systems (CTMS and eTMF tools).
In short, the Clinical Research Associate position at ICON within the FSP framework is a definitive route to transitioning your on-site monitoring experience or nursing background into a high-visibility global asset. Securing an appointment here allows you to move past entry-level support loops and take direct, frontline command of the site compliance reviews, eTMF metrics, and investigator relationships that advance next-generation therapies safely through US clinical pipelines. If you reside in Utah near a major airport hub, meet the 2-year monitoring criteria, and possess a passion for data accuracy, apply today to secure this premier Clinical Research Associate Job, launch an exceptional ICON career, and lock in this outstanding Life Sciences Job.
