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In this role, you will have the opportunity to:Manage a team of Clinical Research Associates assigned to site management and data review of a new cardiac enrollment study, which involves active mentoring, regular coaching, and developing people to build skills and elevate capabilities.
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The Clinical research Data Coordinator is a health professional having a working knowledge ofclinical research activities, communication skills and a willingness to cooperate as a team memberand independently accept the challenge of data management specific to a current protocol.
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Research Practice Manager [RPM], Oncology Clinical Research Unit [OncCRU] Position Description, Occupational Summary Responsible for the oversight of research and day-to-day operations including finances and personnel management for the Brain Tumor Center Clinical Research Program of the Duke Cancer Institute [DCI.
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Incumbent will be supporting Senior Manager to achieve metrics related to activities in support of clinical trials, including design and maintenance of clinical databases using OpenClinica EDC, Veeva ETMF, decentralization tools, SAS; review of data collection forms; generation of data tables, listings and reports; establishment and documentation of data management processes.
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Complies with all applicable regulations, guidelines and procedures pertaining to data loading, EDC and clinical research. Working knowledge of clinical research Electronic Data Capture (EDC) systems.
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Minimum of 3 years’ experience in clinical research and database programming; prefer at least 1 year in device or pharmaceutical clinical trials as a clinical programmer performing mentioned above functions using SAS, Oracle Clinical or Clintrial and/or ACCESS.
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Bachelor’s degree, preferably in areas such as biological sciences, health care management or life sciences research; BSN/RN or experience with management of clinical trials. Participates in assigned activities related to user acceptance testing (UAT) of clinical systems, including EDC and interactive response technology (IRT) and may contribute to the authoring of systems requirements.
$150,000 - $170,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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If assigned, Associate Director, Clinical Operations may act as the Study Team Leader for the assigned clinical study and responsible for leading the cross-functional study team, project managing and coordinating with internal stakeholders to ensure cross functional integration and delivery of study team plan and milestones (e.g. protocol, eCRF/EDC, IXRS, Clinical Study Oversight Plan etc.
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Conduct Clinical Research Coordinator activities for assigned clinical research device studies including consenting participants, conducting study sessions, maintaining device accountability, and completing data entry into the Electronic Data Capture (EDC) system.
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ICON plc is a world-leading healthcare intelligence and clinical research organization. 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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Knowledge of industry standard clinical technologies including CTMS, EDC (RAVE, InForm) Under the Group's 2025 Vision to become a "Global Pharma Innovator with Competitive Advantage in Oncology," Daiichi Sankyo is primarily focused on providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders.
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I-Pharm has specific expertise in Clinical Research, Medical Affairs, Regulatory Affairs, Pharmacovigilance, Quality Assurance and Bioinformatics. Takes a leadership role to gather content and integration requirements for EDC and close collaboration with partners supporting other data collection systems (eCOA, External Data, Safety Gateway.
$130,000 - $170,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The Sr. Clinical Research Associate (Sr. CRA) provides support to Study Lead(s) in clinical study planning, execution and management. Minimum of five (5) years in clinical research and development.
$120,000 - $140,000ExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The candidate will report to Dr. Salomon Amar, VP for Research, and to the Clinical Research Project Manager. Ability to use a combination of validated Electronic Data Capture (EDC) systems and/or other internal or commercial software tools and proven ability to learn and apply new software quickly as projects require.
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This database will store information from EDC, ePRO, Labs, CTMS and other related clinical trial data. Experience working with any leading Clinical Research Organizations (CRO.
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edc clinical research jobs
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