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The Clinical Research Coordinator (CRC) is responsible for the coordination and administration of clinical trials under the direction of the Principal Investigator and Scientific Director.
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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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Ozmosis Research Inc. is an independent, entrepreneurial clinical trials management company in Canada operating as a social enterprise (not for profit). 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 14 days ago - UpvoteDownvoteShare Job
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Handle/manage all duties related to the execution of US/OUS Class 3 Medical Device Clinical Trials in line with GCP, Regulatory and Compliance requirements. This position plays a key role in the development and execution of pre-clinical, feasibility and first-in human trials intended to support regulatory registration of new indications and new medical devices, as well as physician-initiated and company sponsored, and grant funded clinical trials.
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Working in conjunction with the medical affairs and clinical development teams, evaluate potential external clinical research collaboration opportunities and facilitate the conduct of external clinical investigator-initiated trials (IITs) and company-sponsored trials.
$185,013 - $207,311 a yearExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Support ongoing clinical trials by ensuring efficient study execution, data analysis, and serving as a backup Medical Monitor when necessary. Offer clinical and strategic guidance for various study-related documents, including study reports, regulatory filings, protocols, and investigator brochures, working closely with cross-functional teams.
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Assist with Otsuka's clinical trials program, including registrational, post-marketing and Investigator-Sponsored Trials (ISTs), health economic outcomes research, other specific medical collaborations; provide clinical expertise and feedback regarding operational management of clinical trials to ensure optimal site selection and performance.
Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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As a key stakeholder, the Director represents the investigator/research team when working with internal regulatory groups such as the IRB, OCR, Clinical Trials Scientific Review and Monitoring Committee (CTSRMC), Data Safety and Monitoring Committee (DSMC), and DOCM, as well as external entities including pharmaceutical companies, contract research organizations, the FDA, and the NCI's National Clinical Trials Network (NCTN) groups.
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The Clinical Research Coordinator assists the clinical trials process by registering hematology, oncology, and bone marrow transplant patients for clinical studies, assessing eligibility criteria, maintaining current protocol packets and assuring that all quality assurance measures are maintained within the protocol/study.
$39,300 - $64,349 a yearFull-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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The MEL conducts critical activities that support advancing science, educating on evolving clinical practices, transforming science into patient care, and facilitating the development of new research collaborations (including Investigator Initiated Trials and Real-World Evidence.
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Prepares for study visits: research bio-specimen collection order preparation/placement, laboratory and EKG order placement, scheduling of biopsies and scans, facilitating RECIST form completion from the investigator, AE and ConMed form completion in conjunction with a licensed professional (CRN/APP/MD) and other tasks as needed to support the administrative conduct of clinical trials.
$58,500 - $62,000 a yearFull-timeExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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Conduct data review, analyses, and interpretation of clinical trials data together with the GDL, Clinical Safety, and Biostatistics. Responsible for scientific leadership and execution of clinical studies and delivering on innovative clinical study designs, high quality trial execution, investigator engagement, data review, safety assessment, and interpretation of clinical study results.
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We are one of the few pediatric programs with an NIH-funded T32 training grant in pediatric non-malignant hematology•The Aflac Developmental Therapeutics Program offers a wide portfolio of clinical trials from cooperative groups, industry partners, and investigator-initiated studies, and has a larger referral base in the southeastern United States.
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The Stephenson Cancer Center offers over 300 clinical trials encompassing NCI-sponsored, investigator, and pharmaceutical trials. Excellent support and mentorship for grant writing and clinical trials, including a two-year funded master's degree program.
$400,000 - $520,000ExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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As a Research Coordinator, you are responsible for the functions as a back-up to our Study Coordinator in the coordination and participation of clinical research studies conducted by a principal investigator(s) at CenExel CNS in a variety of complex activities involving collection, compilation, documentation, and analysis of clinical research data under the direct supervision of the Principal Investigator.
ExpandApply NowActive JobUpdated 7 days ago
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