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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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Leads, designs and/or oversees eCRF design, eCRF specifications, eCRF completion guidelines, annotated CRFs, User Acceptance Testing (UAT), query logic, edit checks, data query resolution, SAE reconciliation between clinical and pharmacovigilance databases, vendor data reconciliation & cleaning, data migration and database closeout for clinical trials.
$224,000 - $233,000 a yearFull-timeExpandUpdated Today - UpvoteDownvoteShare Job
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NCH is transforming into an Advanced Community Healthcare System(TM) and we’re proud to: Provide higher acuity care and Centers of Excellence; Offer Graduate Medical Education and fellowships; Have endowed chairs; Conduct research and participate in national clinical trials; and partner with other health market leaders, like Hospital for Special Surgery, Encompass, and ProScan.
$10,000 a yearExpandUpdated Today - UpvoteDownvoteShare Job
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With its foundations in engineering disciplines, the companys platforms vertically integrate proprietary hardware, software, bioinformatics, chemistries, and molecular biology to advance basic research, target validation, and clinical trials.
$30 - $34 an hourFull-timeExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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The ideal candidate will have experience/expertise in the development, execution, and management of data collection and data quality review for clinical/health outcomes research studies, clinical trials, and/or digital health research studies.
$80 - $90 an hourFull-timeExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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The Cancer Clinical Trials Office (CCTO) is an integral component of the Stanford Cancer Institute since the vital work performed there enables our adult and pediatric cancer centers to translate research from the laboratory into the clinical setting.
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Knowledge & Other Requirements Knowledge of the drug development process, Good Clinical Practices (GCP) and Good Pharmacovigilance (GVP), including worldwide PV regulations and their application to safety science activities (aggregate PV reports, risk management plans, signal detection, clinical trials and clinical development.
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Experience participating in cross-functional projects and teams with responsibilities related to clinical trials or other drug development activities. Significant experience working in drug safety / PV or a related field in the biopharma industry, clinical research, health administration, health policy, epidemiology, or academic or subspeciality medicine.
$274,635 - $355,410Full-timeExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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Lane Surgery Center represents the pinnacle of precision medicine, combining cutting-edge technologies & innovative patient clinical trials. Lane Surgery Center offers a truly unique opportunity to join a team of award-winning physicians, nurses, surgical technologists, operating room staff, clinical researchers, innovators, educators, and patient advocates at an institution leading the world in medical and surgical innovation to provide the highest level of care to our patients.
$84.84 - $97.87 an hourPart-timeExpandUpdated Today - UpvoteDownvoteShare Job
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Analyze data and interpret results from clinical trials to meet the project objectives; may work on exploratory analyses related to clinical pharmacokinetic/pharmacodynamic, translational biomarker, and/or manufacturing data.
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Lead clinical biomarker, clinical translational research and Dx development in clinical trials and support collaboration research with external academic and clinical partners.
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To lead the process development and GMP manufacturing of Abdera’s novel antibody guided radiopharmaceutical for clinical trials. Manages and leads the CMC process development team for drug substances and drug products from pre-clinical through commercial.
ExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Experience in all aspects of protocol conduct, both early and late phases, including protocol writing, start-up, study execution, analysis, and reporting Sufficient content expertise to be able to meaningfully contribute to document development and data review and interpretation under the direction and oversight of the CMO. Knowledge of applicable FDA Code of Federal Regulations, Good Clinical Practices, and clinical trials guidelines is required.
$250,000 - $315,000 a yearFull-timeExpandUpdated Today - UpvoteDownvoteShare Job
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The candidates will be considered across broad areas of expertise, including clinical trials and/or translational research; the successful candidates are expected to recruit and mentor trainees seeking a career in basic/translational science in endocrinology.
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Responsible for overseeing all facets of early phase clinical trials, from CRO selection, initial startup phase through data base lock in accordance with applicable regulations, ICH/GCP regulations and company Standard Operating Procedures (SOPs.
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clinical trials jobs in Foster City, CA
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