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Using a disease-specific centers model for conducting clinical trials, CRS provides study development and implementation assistance, submissions to the FDA, IRB processing, patient recruitment, study coordination, study-specific training, data collection, and specimen collection and processing.
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Clinical Operations plays a key role in ensuring all client clinical trials are performed in accordance with applicable SOPs, company policies and regulatory guidelines to provide timely and high-quality clinical data that supports global registration and commercialization of clinet products.
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The Clinical Research Services (CRS) team is made up of nearly 200 staff members who facilitate the development, implementation, coordination, internal data monitoring, and completion of oncology-focused trials at Hillman.
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Must have at least 5 years’ experience in fit-for-purpose clinical biomarker assay development, validation, and implementation in support of multi-site clinical trials. The primary responsibilities of this position are 1) to ensure the timely execution of biomarker tests on samples from clinical trials and 2) to perform technical and strategic assessment of new and innovative biomarker platforms.
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Lead Translational Biomarker strategy development and execution to support the clinical stage portfolio, including biomarker driven clinical study design, implementation of novel technologies and incorporation of biomarker endpoints for decision-making in early-stage clinical trials.
$266,200 a yearFull-timeExpandUpdated Today - UpvoteDownvoteShare Job
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Determine, design, communicate and track biomarker diagnostic logistics and planning needs for late-stage clinical trials: This involves assessing the requirements for biomarker implementation and execution and providing assay-related direction to operational teams for seamless integration of biomarker assays at vendors and our Company's labs.
$213,400 a yearFull-timeExpandUpdated Today - UpvoteDownvoteShare Job
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The Clinical Trials Unit currently works on several interventional and observational studies with subjects that have subjective complaints of memory loss, Mild Cognitive Impairment (MCI), Early Onset Alzheimer’s Disease (EOAD), mild to moderate Alzheimer’s Disease (AD), Frontotemporal Dementia (FTD), and semantic variant Primary Progressive Aphasia (svPPA.
$95,595 a yearFull-timeExpandUpdated Today - UpvoteDownvoteShare Job
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With established community partners in the Gulf South, the Center is actively engaged in T3-T4 translational research focused on health outcomes, adherence behaviors, digital health, health equity, and dissemination and implementation research and conducts primarily federally funded (e.g. NIH) clinical trials, observational studies, and secondary analyses of existing databases.
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Under the direction of the Office of Oncology Research Regulatory Affairs and Compliance, the Regulatory Specialist I performs administrative and coordinative work directed toward the design, implementation, evaluation and review of assigned Wake Forest Baptist Comprehensive Cancer Center (WFBCCC) clinical trials by working closely with Principal Investigators and other clinical trial staff members.
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For over 35 years, the Research Center has conducted cutting edge contraceptive clinical trials with a wide range of partners in the public and private sector, including government agencies, non-profit organizations, start-ups, and major pharmaceutical corporations.
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Plays a central role in successful implementation and reporting of single institution and multi-site clinical trials of cell therapy trials for pediatric cancers. The Senior Clinical Research Associate (CRA) will support the Principal Investigator (PI) in conduct of single institution and multi-institution clinical trials of cell therapy.
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In addition, the Cardiovascular Tech II will assist with the evaluation and implementation of new technologies, adherence to protocols for clinical research trials, and support quality based departmental initiatives.
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The Ast. Clinical Research Coordinator will assist with development and implementation of budgets related to clinical trials. The Pelvic Floor Disorders Network (PFDN) conducts a variety of clinical trials (medical, surgical and therapeutic) focused on treatment of women with pelvic floor disorders such as fecal/urinary incontinence and pelvic organ prolapse.
$51.44 an hourFull-timeExpandUpdated Today - UpvoteDownvoteShare Job
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This work is supported by the Cancer Center Clinical Trials Unit, a new cGMP and TCT laboratory, fully characterized tumor samples repository and new state-of-the-art Medical Center opened in 2021, all on the Medical School campus.
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Utilizes professional clinical skills, education and/or experience in project planning and implementation of data collection for complex clinical/health research trials. Certifications, licenses, or degrees as determined by the needs of the research projects, such as, registered nurse, nurse practitioner, certified mental health therapist/specialist, MSW, pharmacist, physical therapist, certified health education specialist, clinical psychologist, acupuncturist.
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clinical trials implementation jobs
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