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Improving Supportive Care for Patients with Thoracic Malignancies is a 3 year funded trial by Genentech to evaluate the impact of a lay health coach on symptom management. LUNGEvity is a 2-year funded trial to evaluate the impact of a lay health coach on precision cancer care delivery for patients with lung cancer.
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Reporting to the Clinical Research Manager of Blood & Marrow Transplantation and Cell Therapy (BMT-CT), the Clinical Research Coordinator Associate will be conversant in the goals, mission and priorities of the Institute, and utilize this knowledge to to manage data, enroll and follow patients on trial, and assist with regulatory and financial requirements of the trials.
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CARGO is currently evaluating its lead program, CRG-022, an autologous CD22 chimeric antigen receptor (CAR) T-cell therapy candidate, in a potentially pivotal Phase 2 clinical trial in patients with large B-cell lymphoma (LBCL) whose disease relapsed or was refractory (R/R) to CD19 CAR T-cell therapy.
Full-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Provide support in production or validation of summary tables, data listings and graphs required for trial report and clinical development, and CDISC data sets for regulatory submission. This position requires a comprehensive knowledge of CDISC standards, clinical trial study design, and electronic data submission requirements.
$160,000 - $175,000 a yearFull-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Ensure inspection-readiness for all assigned studies, including ensuring all components of the trial master file (TMF/eTMF) are up to date and accurate. Innova Solutions is immediately hiring for a Contract Clinical Trial Manager-Sr. Clinical Trial Manager Position type: Full-time Contract Duration: 6 - 12 month Location: Hybrid role in Redwood City, CA - 3 days onsite As Contract Clinical Trial Manager-Sr. Clinical Trial Manager you will: Job Description This is an exciting opportunity to work within a fast-paced environment with a dedicated, passionate, intelligent team.
$70 - $80 an hourExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Reporting to the Head of Statistical Programming, the Associate Director is responsible for the planning, execution, and quality of SAS programming to conduct statistical analyses in support of clinical trial results.
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Review complex clinical trial and CDMO accrual models; ensure accounting treatment is in accordance with US GAAP. Reporting to the Corporate Controller, CARGO Therapeutics is hiring an Associate Director, Accounting.
Full-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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BA or BS and 12+ years’ experience in compliance and trial master file in pharmaceutical/biotechnology industry. The Associate Director, Clinical Records & Information Management will partner with cross functional teams as well as Clinical Research Organization (CRO and Functional Service Provider (FSP) to ensure timely and quality delivery of the TMF. This role is a member of the Clinical Records leadership team to ensure optimum implementation of the TMF technical capabilities and oversight of standardization, training, quality, and timely clinical trial documentation across the clinical program.
$191,335 - $247,610 a yearExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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The ideal candidate will possess substantial litigation and/or trial experience, strong legal writing skills, and a proactive approach. Substantial litigation and/or trial experience preferred.
Full-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Reviews and analyzes safety reporting, biomarker analyses and other aspects of clinical trial monitoring. This may include, but is not limited to, providing statistical consultation on clinical development plans, clinical trial design and clinical study endpoints, calculating sample size, authoring statistical analysis plans and providing biostatistical input into clinical development documentation, scientific publications and presentations, and regulatory filings.
$165,580 - $214,280Full-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Experienced litigation attorney: You’ll manage the entire legal process, from investigation and discovery though trial prep and court proceedings representing clients in depositions, site inspections, court hearings, trials, etc.
Full-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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The Clinical Trial Manager provides operational leadership to ensure the study milestones are delivered on time, within budget, with high quality, and in compliance with the ICH/GCP, Regulatory Authorities' regulations/guidelines, and applicable SOPs.
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We are seeking an experienced and organized Trial Master File (TMF) Manager to oversee and lead the development and management of Iovance TMF. The TMF Manager serves a key role, working across the business for the execution of TMF Operations processes and strategy.
Full-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Thorough understanding of clinical trial design and reporting processes, and regulatory reporting requirements including electronic data submissions, and CDISC implementation. Thorough understanding of clinical trial design and reporting processes, and regulatory reporting requirements including electronic data submissions, and CDISC implementation.
ExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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We offer rapid, dedicated stroke MR and CT imaging meant to differentiate between completed stroke and “at-risk” tissue, with automated decision support software that has been validated in multicenter trial.
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trial job in Palo Alto, CA
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