As a Senior Clinical Data Science Lead you will be joining the world's largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
What you will be doing: Take part in study kick off (internal and external) meeting along with the DMPMRead, ensure understanding and adhere to the study protocol, contract and scope of work for all task during set-up, maintenance and close-out of the studyAssist the DMPM with revenue recognition and revenue forecasting process on a monthly basisLead the development of specifications, implementation, and testing for the eCRF or paper CRFLead the development of specifications, implementation, and testing for the edit checks and data review and oversight listings (DVS)Lead development of the data management plan and study specific proceduresEnsure effective implementation of standard metric and status reporting on the studyLead development of specifications for custom reporting on the studyPerform project-planning tasks and support the DMPM in the development of the project plan and timelinesSet up and maintain data management study files for inclusion in the Trial Master File, ensuring these are maintained in an audit ready state for review by Sponsor, Regulatory or ICON AuditorsAdhere to the project plan and timelines in the implementation of study tasks during set-up, maintenance and close-out of the studyKey point of contact for the sponsor and the study team on day to day study data issues, eCRF design, edit checks, and other implemented componentsOrganize and lead regular data management team meetings, both internal and with the sponsor and the DMPMAttend and provide an update for data management services at cross-functional study team meeting both internally and with the sponsor and the DMPMMaintain and track meeting minutes, issues and decisions logs, and escalations You are: Bachelor's degree preferred, preferably in a scientific discipline such as Statistics, Mathematics, Economics, Computer Science, IT, Biology, Social Science, etc.4+ years of Clinical Data Management experienceRobust experience with EDC (E.g. Medidata Rave) and use of Data Review tools such as elluminate, J-Review or Business Objects requiredDeep understanding of drug development and biopharmaceutical industry requiredStrong technical skills, including experience working with using Microsoft Excel functionalityExcellent written and oral communication skillsWhat ICON can offer you: Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our benefits examples include:
Various annual leave entitlementsA range of health insurance offerings to suit you and your family's needsCompetitive retirement planning offerings to maximise savings and plan with confidence for the years aheadGlobal 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-beingLife assuranceFlexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among othersAt ICON, diversity, inclusion & belonging are fundamental to our culture and values. Our rich diversity makes us more innovative which helps us better serve our people, patients, customers, and our communities. We're proud of our diverse workforce and the work we've done to become a more inclusive organisation. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below.
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