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The Clinical Affairs Director for Beckman Coulter Diagnostics is responsible for leading comprehensive global clinical trial strategies to support the complex Clinical Chemistry and Immunoassay Biomarker-Flywheel (Biomarker) program and for managing a multi-level team of clinical managers and clinical scientists/affairs associates.
$117ExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Assist with equipment installation, trial runs, investigative tests, repairs, and overhauls of building automation systems. They are an integral part of our Business Conduct Guidelines and our corporate strategy electrical wiring, wiring, conduit, wire, cable, panel, sensor, pipe, electronic, electric, electrical, low-voltage, low voltage, building automation, hvac controls, hvac, fire alarm, security systems, cctv.
ExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Draft project specific TMF Plan and structure at the beginning of the trial as well as maintain and update TMF plan throughout the trial. 2-3 years of experience in trial master file.
ExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Systems may include: - Clinical Trials Management System (CTMS); Business Intelligence (BI) and dashboards for CTMS; electronic Trial Master File (eTMF); Electronic Data Capture (EDC)/ Thesaurus Management System (TMS) and underlying systems; Clinical Outcome Assessment Repository (COAR); Metadata Repository (MDR); Clinical Data Repository (CDR); Electronic Document Management System (EDMS); and others.
ExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Our offerings include source testing for routine regulatory compliance, engineering studies, control device evaluations, MACT demonstrations, relative accuracy test audits (RATAs), and trial burns; ambient air monitoring; temporary continuous emissions monitoring systems (CEMS); and advanced testing capabilities in Fourier Transform Infrared Spectroscopy (FTIR) and gas chromatography.
Full-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Summary: The Clinical Research Nurse Coordinator promotes the mission of Accellacare to function as an Integrated Site Network providing unparalleled service to our clinical trial partners. Completes training on Clinical Trial Management System and maintains proper skills to update database, complete participant reimbursement, capture referral source of participants, and create calls lists to promote recruitment.
Full-timeExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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Excellent understanding of the clinical research process, including US FDA, EU, and GCP regulations, and the function of quality control in clinical trial conduct. Compile and report quality metrics, building effective relationships with internal and external customers and ensuring continuous improvement in the conduct of clinical trial activities.
ExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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Why LMK: LMK Clinical Research Consulting is a recognized leader in Trial Master File (TMF) document management services and solutions for the life sciences industry. What You Will Be Doing: LMK’s TMF Support Analyst is the Quality Control Expert and ensures accuracy and completeness of all clinical documentation within the TMF. The clinical trial documentation must be consistent with the Trial Master File Specifications, submission/inspection readiness criteria and comply with LMKs (or clients) SOPs and regulatory requirements.
ExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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In addition to the 52 shortened weeks from the 4 Day Work Week trial, Workshop Digital provides: 2-3 weeks personal vacation time off, 5 sick days, and several holidays including MLK Day, Labor Day, Memorial Day Thanksgiving, Christmas Day, and your birthday.
Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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JOB SUMMARY: The CTMS Business Analyst is responsible for providing high-quality calendar builds and accurate financial entry services (service deliverables) for site clients who utilize a Clinical Trial Management System for clinical research financial oversight and patient enrollment management.
RemoteExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Demonstrated understanding of the overall drug development process with clinical trial design, study implementation, sponsor/site interactions, scientific and clinical methodology, protocol design, project management and regulatory requirements for clinical studies to be reviewed by health authorities.
ExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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Dashboards for CTMS; electronic Trial Master File (eTMF); Electronic Data. dashboards for CTMS; electronic Trial Master File (eTMF); Electronic Data. Clinical Outcome Assessment Repository (COAR); Metadata Repository (MDR.
ExpandApply NowActive JobUpdated 13 days ago - UpvoteDownvoteShare Job
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MMS is an innovative, data-focused CRO that supports the pharmaceutical, biotech, and medical device industries with a proven, scientific approach to complex trial data and regulatory submission challenges.
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Ensure Medical is a proactive partner with Development through cultivation of relationships across Global Medical, CSU, R&D, EDO, GPT, CSO leadership to ensure all Medical activities are aligned with Sanofi US clinical trial goals.
ExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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This is a multi-faceted role for an experienced candidate whose efforts will streamline existing clinical trials and substantially impact the use and re-use of clinical trial data for increased efficiency and insight.
ExpandApply NowActive JobUpdated 15 days ago
trial job in Raleigh, NC
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