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This position is part of the Chemical Chemistry and Immunoassay (CCIA) Clinical Affairs department located in Chaska, Minnesota and can be remote. Accountable for planning, design, execution, and results of the Clinical Affairs Biomarker team & clinical trials program.
$185,500 - $235,500 a yearFull-timeExpandApply NowActive JobUpdated 15 days ago - UpvoteDownvoteShare Job
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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.
$185,500 - $235,500 a yearFull-timeExpandApply NowActive JobUpdated 17 days ago - UpvoteDownvoteShare Job
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Interactswith HCPs as a scientific resource to support activities aligned with the Medical Plan including advisory boards, speaker development and clinical trials. Collaborate with medical affairs and clinical organization to support patient enrollment in our company's sponsored clinical trials with site recommendations.
$160,000 - $210,000 a yearFull-timeRemoteExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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CfOR studies include but are not limited to evidence generation regarding the frequency and distribution of disease, the clinical burden of disease, the natural history or clinical course of disease, the design of clinical trials, treatment cost and utilization patterns, and the safety and effectiveness of therapeutic interventions.
Full-timeRemoteExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Veeva Systems is looking for Senior Consultants who have life sciences software programming experience specifically in helping customers optimize the use of EDC in running their clinical trials.
$80,000 - $200,000 a yearFull-timeRemoteExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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Through innovative treatments, cutting edge technologies and our research network we work to deliver the best cancer care to our patients, including participation in clinical trials leading to over 100 FDA approvals.
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Work with MGB Research Management, Clinical Trials Office (CTO) and Innovation offices to manage lifecycle of research grants and contracts. Maintain working knowledge of federal Human Subjects System (HSS) and Clinical Trials.gov to assist with entry and troubleshooting of clinical trials and human subjects data.
RemoteExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Act as a Quality Program Lead on clinical trials by supporting national and international regulatory standards and guidance for pharmaceuticals, biologics and medical devices. Develop audit management plans and audit strategy with clients for ongoing clinical trials.
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Experience with Internal Review Board (IRB) processes, USDA, and clinical trials. We offer flexible working hours, remote work options, and other initiatives to help you achieve a harmonious integration of work and personal life.
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We are seeking a ClinicalProject Manager to join our Project Management Office (PMO) Team responsible for project management, cross-team coordination, and delivery of new clinical trials projects.
Full-timeExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Lead biomarker and pharmacokinetic planning, definition, and implementation, overseeing sample collection for early and late-phase clinical trials. Senior Director, Clinical Biomarkers - Permanent - Remote.
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Extensive oncology experience, including proficiency in target/disease biology, preclinical, and clinical development. Develop strategic plans to meet budgetary requirements and successfully integrate companion diagnostic assays into end-of-life trials.
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Proclinical Staffing is seeking a Senior Director, Clinical Biomarkers to join an innovative biotech company. Develop and enforce operational standards for biomarker management, vendor relations, and internal processes to ensure program quality, efficiency, and regulatory compliance.
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Professional Knowledge: Thorough understanding of diagnostic technologies, global regulatory frameworks, and biomarker applications in drug development. Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
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Engage with external diagnostic providers and global regulatory agencies to establish CDx filing pathways and compliance strategies. Education: PhD degree in Biology, Translational Medicine, or related life sciences areas.
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