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Manages and coordinates all facets of assigned clinical protocols from IRB preparation through query and data seal; ensuring protocol and regulatory compliance. The Ivy Brain Tumor Center is a non-conventional, non-profit program offering state-of-the-art clinical trials for patients with the most aggressive form of brain cancer.
$30.55 - $44.3 an hourFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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The Research Nurse Coordinator is responsible for ensuring that the clinical research is conducted according to the research design including but not limited to screening and recruitment of patients, collecting and records of clinical data, maintaining regulatory binders and overall safety of human subjects.
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The Medical Director is responsible for global pharmacovigilance (PV) for marketed and/or investigational products, including review and analysis of safety data from post-marketing sources and from clinical trials, the identification and investigation of safety signals, management of benefit-risk profile for assigned compounds and products.
Full-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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5+ years’ experience working with EDC clinical software solutions in end-to-end data management related activities (database design, data collection, data analysis, query resolution, datasets, statistical reporting.
$80,000 - $200,000 a yearFull-timeRemoteExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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This person will work flexibly across a number of clinical stage trials and projects, acting as a study lead and manager for select clinical trials, and be hands-on in data compilation, review and analysis, clinical trial set-up and management, and operational support activities.
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Demonstrated knowledge of all components of the research process as it pertains to clinical trials and studies, i.e., IRB procedures and processes, data management. Demonstrated organizational skills to efficiently and effectively support multiple clinical trials and projects, providing accurate information in a timely manner.
$24.28 an hourFull-timeExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Thorough knowledge of clinical research concepts, practices, FDA regulations and ICH guidelines regarding drug development and data management methods. Ensures timely conduct of clinical studies according to protocols, Good Clinical Practice (GCP), Standard Operating Procedures (SOPs), and all applicable regulations and guidelines governing the conduct of clinical trials.
$150,000 - $170,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Knowledge of data management principles and regulatory requirements for clinical trials and medical research. Participates in the design, development, and reporting of research studies and clinical trials.
Full-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Experience with statistical applications and clinical data management procedures in the conduct of clinical trials. Ability to effectively represent Biostatistics and Clinical Data Management in multidisciplinary meetings.
$112ExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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You will focus on projects from the start of assay development to clinical trial implementation as well as data management to ensure we are obtaining high-quality data from our clinical trials.
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Ensure Global clinical trials case reporting process is efficient and compliant with reporting requirements detailed in the safety management plans (SMP) / PV agreements Support the oversight and management of global business partner safety data exchange agreements/ pharmacovigilance agreements and other contracts as applicable to ensure compliance with data exchange activity.
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The Senior Clinical Trials Manager provides oversight of the CRO and other third-party vendors on their assigned study as well as expertise to internal teams (regulatory affairs, medical writing, biometrics, pharmacovigilance, and product manufacturing) to ensure quality processes and deliverables.
$155,000 - $165,000 a yearFull-timeExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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RESPONSIBILITIESThe Clinical Trials Specialist (CTS) participates in the development, coordination, data and project management of clinical trials from protocol development/review, approval through to activation, follow-up and trial closure.
ExpandApply NowActive JobUpdated 15 days ago - UpvoteDownvoteShare Job
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Drive study related activities from pre-clinical/clinical protocol design to Human Factors input, data management, study start-up/execution/close-out for one or several studies.
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5+ years of experience working with EDC clinical software solutions in end-to-end data management related activities (database design, data collection, data analysis, query resolution, datasets, statistical reporting.
$80,000 - $200,000 a yearRemoteExpandApply NowActive JobUpdated 7 days ago
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