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Overview ICON plc is a world-leading healthcare intelligence and clinical research organisation. At ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises not only an excellent level of base pay, but also a wide range of variable pay and recognition programs.
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Ripcord customers include global enterprises such as Coca-Cola, IRS, Allianz Insurance, and MUFG. We’re based in the Bay Area, California and are backed by the world’s leading investors including Kleiner Perkins, Google Ventures, Lux Capital, Icon Ventures, Silicon Valley Bank, Apple co-founder Steve Wozniak and more.
$125 - $150Full-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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ICON Plc has a fantastic opportunity for a Client Relationship Manager to join our team. ICON plc is a world-leading healthcare intelligence and clinical research organisation.
$108,144 - $135,180 a yearFull-timeExpandUpdated 1 month ago - UpvoteDownvoteShare Job
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ICON plc is a world-leading healthcare intelligence and clinical research organization. In addition to your competitive salary, ICON offers a range of additional benefits. What ICON can offer you: Our success depends on the quality of our people.
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ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. We would encourage you to apply regardless - there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.
Full-timeRemoteExpandApply NowActive JobUpdated 21 days ago - UpvoteDownvoteShare Job
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ICON people have a mission to succeed and a passion that ensures what we do, we do well. Are you a current ICON Employee? From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organizations.
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Visit our careers website to read more about the benefits of working at ICON https. What ICON can offer you. The Senior Statistical Programmer provides support to the lead programmer and study team on all programming activities according to the study requirements and the timelines.
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As a CRA II or Senior Clinical Research Associate at ICON, you’ll work within a large-scale, fast-paced environment alongside a close-knit team of highly qualified CRAs to identify, select, initiate and close-out investigational sites for clinical studies in phases II - IV, ensuring adherence to applicable regulations and principles of ICH-GCP.
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2+ years of project management and vendor management experience. InForm EDC experience. Coordinate resolution & risk mitigation of all ePRO / eCOrelated issues and end-of-study vendor deliverables. Experience in executing UAT Scripts and/or Change Requests.
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Visit our careers website to read more about the benefits of working at ICON: including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment.
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What you will be doing:The Senior Statistical Programmer provides support to the lead programmer and study team on all programming activities according to the study requirements and the timelines. MS. (BS) in Statistics, Computer Science, Mathematics, Engineering, Life Science, or related discipline with 3+ (4+) years of programming experience preferably in processing clinical trial data in the biotechnology, pharmaceutical or health related industry.
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Good understanding of standards specific to clinical trials such as CDISC, SDTM, ADaM, MedDRA, WHODRUG. BS/MS in Statistics, Biostatistics, Computer Science, Mathematics or Life Sciences - 10+ years of statistical programming experience in the Pharmaceutical, Biotechnology, or Contract Research Industry.
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The Sourcing Manager is to support commercial marketing Strategic Sourcing to ensure successful sourcing responsibilities such as, risk mitigation, contract review and negotiations, supplier relationship management and compliance to corporate policies.
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Work with PI to develop and implement recruitment strategies in accordance with IRB/IEC requirements. Manage the investigator file (ISF) and other regulatory documents throughout the study by obtaining essential documentation and complying to regulatory and sponsor requirementsParticipate in the SIM, site activation visits (SAV) and interim monitoring visits.
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Visit our careers website to read more about the benefits of working at ICON: (url removed) xml, Reviewer’s Guide and analysis metadata report, executable programs for CRT packages. Independently develop accurate and CDISC compliant ADaM specifications.
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