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Reporting directly to the Translational Project and Lab Manager, the Translational Research Coordinator I supports the clinical research efforts of the MCC by providing comprehensive coordination and data management for a portfolio of translational research protocols.
$31.04 - $49.94 an hourFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Reporting to the Clinical Research Manager of Cancer Cell Therapy (CCT), 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.
$27.88 - $36.54 an hourExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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The primary responsibility of the Clinical Research Coordinator B (CRCB) in the Department of Ophthalmology is to implement one or more industry sponsored, NIH or investigator initiated clinical trials assuring each study is conducted per protocol and adheres to ICH/GCP guidelines.
$43,919 - $66,183 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Reporting to the SVP of Clinical Development & Operations, the Director/Senior Director of Clinical Bioanalytical provides leadership in the development and qualification/validation of analytical assays used in the clinical trials of AAV-based gene therapy programs.
$130Full-timeExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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Additionally, under the Research Compliance Office at HCI , the person in this position will oversee and manage activities related to data on IITs at HCI in the center’s clinical trials management system (OnCore®), which in turn serves as the primary source of data for reporting to the center leadership, ClinicalTrials.gov, and National Cancer Institute ( NCI ) CTRP.
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At Science 37 Atlanta, Georgia - Remote Science 37 is accelerating the research and development of breakthrough biomedical treatments by bringing clinical trials to patients' homes. Provide regular reporting on the current status of the security program to the senior leadership team and the board of directors as part of a strategic enterprise risk management program.
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We have built a deep portfolio of AVV-based gene therapy product candidates, with five product candidates in clinical trials: 4D-150 for the treatment of wet age-related macular degeneration (wet AMD) and diabetic macular edema (DME), 4D-710 for the treatment of cystic fibrosis lung disease, 4D-310 for the treatment of Fabry disease cardiomyopathy, 4D-125 for the treatment of X-linked retinitis pigmentosa (XLRP), and 4D-110 for the treatment of choroideremia.
$128,000 - $149,000 a yearFull-timeExpandApply NowActive JobUpdated 2 months ago - UpvoteDownvoteShare Job
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Northside Hospital Cancer Institute's (NHCI) Cancer Research Program is one of the largest community-based oncology/hematology programs in the nation and is one of the few cancer research programs in the country offering Phase I-IV clinical trials.
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Together with Clinical Sciences and Clinical Operations, provide drug safety oversight of clinical programs including planning, execution, and completion of clinical trials according to all applicable regulations and guidance, ICH/GCP, and Crinetics SOPs.
$319,500 - $426,000 a yearFull-timeExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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The Clinical Safety Scientist will provide operational and scientific support in managing the development, implementation and oversight of Arrowhead investigational products with engaging in, but not limited to: support safety governance and surveillance procedures including safety reporting processes, advanced safety analytics, expedited and periodic aggregate reports ensuring compliance with internal standard operating procedures, FDA and global safety reporting requirements.
$85Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Work on complex projects, provide clarity, create and assess business cases for clinical trials, carry out in depth analysis, support negotiation by performing financial modelling/analysis on investment decisions.
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The Clinical Trials Regulatory Specialist I is an entry-level position supporting regulatory affairs in clinical trial research. Supports processes and monitors practices to ensure regulatory documentation involving clinical trials complies with Institutional Review Board (IRB) policies and procedures and regulations.
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We are using models early to fail less often, executing clinical trials to add valuation to the company, and generating fit-for-purpose data to feed back into Valo’s Opal Computational Platform™ as we reinvent drug discovery and development from the ground up.
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Prepare and submit proposals for new Aids Clinical Trial Group/HIV Prevention Trials Network contracts ensuring that all applicable direct and indirect cost rates are applied. Perform monthly reconciliation for several CIDI - CCGHE-ID grants and contracts using SAP, Analysis and other institutional reporting systems.
$62,300 - $109,000 a yearExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Solid knowledge and experience of industry standards applicable to clinical study data and reporting on clinical trials, including CDISC standards. Work collaboratively with Clinical Development team or CRO to meet project deliverables and timelines for statistical data analysis and reporting.
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