Remote Clinical Research Job at ICON, UK | Life Sciences | Apply Online
If you are an ambitious clinical operations professional looking to transition into international study management, this full-time Clinical Research Job is an exceptional match. ICON plc is currently onboarding a remote Global CTA to support its expanding Early Phase Services division out of the Reading, UK hub. Securing this position provides a high-visibility global platform to manage multi-country study timelines, affiliate budgets, and end-to-end trial lifecycles. It serves as an elite launchpad for a long-term ICON career and stands out as a premier choice for professionals tracking a high-growth, remote Life Sciences Job.
About The Company
ICON plc is a world-leading global healthcare intelligence and Contract Research Organization (CRO). We are 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. Through our specialized Functional Service Provider (FSP) framework, we partner directly with top-tier pharmaceutical sponsors to accelerate the delivery of safe, effective medical therapeutics. Driven by a culture of excellence, this Clinical Research Job rewards high performance and actively nurtures global talent.
Clinical Research Job – Key Responsibilities
As a Global CTA, you will provide critical support to local project management activities, overseeing the country-level operational aspects of assigned clinical trials from initial start-up through to final closeout.
Your core data, administrative, and tracking duties will include:
- End-to-End Project Support: Assisting senior managers in the planning, execution, and remote monitoring of international clinical trials to ensure complete alignment with protocol requirements, regulatory guidelines, and ICH-GCP standard operating procedures.
- Financial & Budget Reconciliation: Assisting in the daily management of project budgets and country affiliate spending, reconciling vendor invoices, tracking final budgets, and liaising directly with Accounts Payable.
- Cross-Functional Collaboration: Partnering with cross-functional global squads, including Clinical Operations, Data Management, and Biometrics, to support successful trial execution and eliminate operational bottlenecks for this remote Life Sciences Job.
- Meeting & Repository Governance: Scheduling study management team meetings for each assigned international project, compiling technical minutes, and archiving documentation precisely in designated central repositories.
- Site Coordination Logistics: Supporting local site activities including site initiation visits (SIV), patient recruitment acceleration initiatives, and data collection timeliness to ensure high-quality documentation.
- Study Close-Out Management: Facilitating essential trial close-out activities, including comprehensive data cleaning, discrepancy analysis, and the formal preparation of final clinical study reports (CSR) to elevate your ICON career.
Profile Requirements & Qualifications For Remote Clinical Research Job
This international position is meticulously tailored for analytical professionals who demonstrate a strong command of multi-country trial documentation and compliance tracking.
- Educational Foundation: A Bachelor’s or advanced graduate degree in Life Sciences, Health Sciences, or a closely related quantitative scientific field.
- Industry Track Record: Proven previous experience working in clinical research or healthcare operations within the pharmaceutical, biotechnology, or Contract Research Organization (CRO) sector.
- Geographic Scope: Verifiable experience operating in a similar trial assistant or coordination role that spans across multiple countries simultaneously to qualify for this global Clinical Research Job.
- Core Competencies: Exceptional organizational habits and sharp time-management skills, with a demonstrated ability to prioritize competing milestones effectively.
- Analytical Skills: Strong attention to detail, proactive problem-solving abilities, and an unyielding commitment to data accuracy, clinical integrity, and quality compliance.
- Communication Style: Effective interpersonal communication skills, with a natural ability to collaborate cross-functionally and build strong relationships with global study teams and clinical trial sites.
In short, applying for this Global CTA vacancy is a definitive route to transitioning your localized trial tracking skills into a highly marketable, international operations portfolio. Securing this remote Life Sciences Job allows you to step away from isolated, single-site administration and manage the macroeconomics, vendor networks, and cross-functional data streams that steer multi-national clinical trials. If you possess a relevant scientific degree, multi-country coordination experience, and the drive to work autonomously, apply today to secure this premier opportunity and build a lasting ICON career.
