Job Url: https://www.remoterocketship.com/company/iconplc-6/jobs/clinical-data-science-lead-united-states Job Description: ICON plc Website LinkedIn All Job Openings ICON plc is a leading global provider of outsourced development and commercialisation services to the pharmaceutical, biotechnology, medical device, and government industries. Offering a comprehensive range of services including clinical trial management, regulatory affairs, and market access solutions, ICON leverages advanced technologies and innovative methodologies to improve the efficiency and effectiveness of drug development processes. With a strong commitment to patient-centered approaches and a focus on therapeutic areas like oncology and rare diseases, ICON is dedicated to transforming clinical research to deliver better healthcare outcomes. Medical Device • Therapeutics • Government and Public Health Solutions • Clinical Research Services • Commercialisation and Outcomes 10,000+ employees 🧬 Biotechnology 💊 Pharmaceuticals ⚕️ Healthcare Insurance Clinical Data Science Lead 7 hours ago 🇺🇸 United States – Remote ⏰ Full Time 🟠 Senior 📊 Data Scientist Apply Now Receive Emails with Similar Jobs Report problem 📋 Description • Participates in study level vendor oversight activities. • May represents data management function on the Clinical Sub-team ensuring aligned expectations between the CRO and client for all data related deliverables, especially in support of key decision points and regulatory submissions. • Serves as a first point of contact for CROs partners when collaboration is needed to ensure established milestones and deliverables are met with the highest degree of quality. • Partners with appropriate stakeholders and CRO partners to mitigate and resolve risks. • For studies where data management activities are conducted within client, leads and manages clinical trial data collection set-up, data review, and database lock: (a) Works with other functions to complete set up of EDC and other study data collection tools such as IRT, ePRO and eCOA. (b) Leads the creation and maintenance of study data cleaning plan components, including edit checks (data validation plan), listing review checks, data integration specifications, data transfer specifications, external data reconciliation plan(s), coding guidelines, SAE reconciliation guidelines, database lock plans. (c) Leads data review, including query management, and leads activities required for interim and final database locks. • Participates in preparing function for submission readiness and may represent function in a formal inspection or audit. • Ensure archival and inspection readiness of all Data Management Trial Master File (TMF) documents. • Tracks study deliverables and evaluates study metrics to mitigate risk for major data management deliverables and milestones. • Responsible for the planning and management of external Data Management budgets and timelines to ensure accuracy, understand trends in variances and support continuous improvement in forecasting. • May prepare metrics to support the function’s KPIs. • Represents function in external professional initiatives and organizations such as SCDM, CDISC, DIA, etc. to identify industry best practice and increase the visibility of client. • Contributes to functional Continuous Improvement initiatives, providing expertise and ensuring deliverables are provided on time, to budget, and in alignment with company, departmental or functional requirements. • Works cross-functionally to ensure the quality of the data in each database and on time delivery, as well as quality of other data management deliverables • Champions and adopts technology improvements and tools for use in clinical data management processes. • Ensure compliance with own Learning Curricula, corporate and/or GXP requirements. • Performs other duties as assigned. 🎯 Requirements • BS/BA required preferably in a health-related, life science area or technology-related fields. • Preferred 4 plus years or experience in data management and/or drug development process with expertise in the cross-functional interfaces with the data management function. • Proven track record of strong project management skills and experience managing data management activities for large drug development programs. • NDA/CTD Experience preferred. • Strong knowledge of data management best practices & technologies as applied to clinical trials. • Solid understanding of clinical trial documents (protocols, statistical analysis plans, CRFs, study reports) and processes. • Strong knowledge of FDA and ICH regulations and industry standards applicable to data capture and data management process. • ecoa experience required 🏖️ Benefits • Various annual leave entitlements • A range of health insurance offerings to suit you and your family’s needs • Competitive retirement planning offerings to maximise savings and plan with confidence for the years ahead • Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being • Life assurance • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others Apply Now