Remote Clinical Research Job at ICON, USA | Life Sciences | Apply Now
If you are an experienced clinical monitor or a qualified registered nurse looking to apply your trial oversight skills within a world-class global network, this position at ICON plc is an exceptional opportunity. Strategically aligned with the ICON Strategic Solutions division, this home-based role allows you to combine remote data curation with critical on-site investigator clinic management. For relationship-driven monitors searching for a high-impact Clinical Research Job, this position offers end-to-end operational ownership of multi-center clinical trials, patient safety auditing, and regional site management. It serves as an elite milestone for a long-term ICON career and stands out as a premier choices for anyone tracking a high-growth Clinical Research Associate Job within the sophisticated United States pharmaceutical sector.
About The Company
ICON plc is a world-leading global healthcare intelligence and Contract Research Organization (CRO) driven by a unified mission to accelerate the development of innovative drugs and medical devices. Headquartered in Dublin, Ireland, with massive operational hubs across the United States, ICON manages centralized laboratory services and decentralized clinical testing footprints spanning multiple continents. This specific role sits within ICON Strategic Solutions, operating under a Functional Service Provider (FSP) framework. In this highly collaborative model, you are deployed directly into a single, top-tier global pharmaceutical sponsor’s pipeline. This unique infrastructure grants you the ultimate benefit of focusing deeply on the sponsor’s specific protocols and cross-therapeutic compounds, backed by the comprehensive corporate benefits, training platforms, and administrative stability of ICON.
Clinical Research Job – Key Responsibilities
As a Clinical Research Associate, you will serve as the primary technical point of contact between regional investigational sites and the pharmaceutical sponsor, ensuring that all clinical data streams are executed in total alignment with international regulations.
Your core monitoring, patient safety, and data compliance duties will include:
- Full-Lifecycle Site Visits: Executing all essential site monitoring phases—including Site Selection (SQV), Site Initiation (SIV), Routine Interim Monitoring (IMV), and Close-Out Visits (COV)—across the assigned Southeast region.
- GCP Compliance Verification: Reviewing site operations, source documents, and data logs to ensure absolute compliance with ICH-GCP guidelines, sponsor SOPs, and Code of Federal Regulations (CFR) frameworks.
- Patient Safety Oversight: Reviewing clinical records to monitor patient safety, ensuring the timely, accurate documentation and reporting of Adverse Events (AEs), Serious Adverse Events (SAEs), and Product Quality Complaints (PQCs) to advance this Clinical Research Job.
- Systems & Trial Master File Governance: Maintaining up-to-date, audit-ready clinical trial documentation across central Clinical Trial Management Systems (CTMS) and electronic Trial Master File (eTMF) platforms.
- Investigational Product Accountability: Overseeing site-level drug accountability logs, verifying proper environmental storage conditions, and managing the compliant return or destruction of investigational products.
- Data Query Resolution: Auditing electronic case report forms (eCRFs), resolving complex data queries, and driving site personnel to achieve timely, high-quality data entry to support this Clinical Research Associate Job pipeline.
Qualifications & Profile Requirements For Clinical Research Job
This corporate position is systematically tailored for analytical, highly organized communicators who possess the technical confidence to build exceptional rapport with site investigators and manage multiple protocol timelines.
- Educational Foundation: A formal Bachelor’s degree in a Life Sciences discipline, or equivalent qualification, or a fully licensed Registered Nurse (RN) designation.
- Industry Track Record: A minimum of 2+ years of independent, on-site monitoring experience operating within the pharmaceutical, biotech, or CRO industry.
- Therapeutic Adaptability: Proven clinical trial exposure across multiple therapeutic areas; experience monitoring Immunology protocols is highly preferred to accelerate your ICON career.
- Travel Flexibility: Willingness and ability to travel up to 50% for on-site monitoring visits. Preference will be given to candidates residing in the Miami, FL area near major HUB airports to facilitate efficient regional transit.
- Legal Authorization: Applicants must be permanently authorized to work in the United States indefinitely without requiring current or future corporate visa sponsorship.
In short, the Clinical Research Associate position at ICON is a definitive route to transitioning your foundational clinical trials or nursing background into a globally recognized operations asset. Securing this appointment allows you to bypass transactional data logging and take direct operational charge of the site relationships, patient safety metrics, and eTMF configurations that drive breakthrough therapies into global medical markets. If you reside in South Florida, meet the 2-year on-site monitoring threshold, and possess a passion for data integrity, apply today to secure this premier Clinical Research Job, launch a highly rewarding ICON career, and lock in this outstanding Clinical Research Associate Job.
