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Performs study start-up duties including the production of a recruitment tool, and progress notes, as well as phone screening patients and identifying participants for trials on site.
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Demonstrated experience in research protocol start-up procedures, including: study feasibility, study activation and IRB processes, and qualification procedures. Under general supervision, the Trauma/Burn Clinical Research Assistant works with UCSD faculty and principal investigators in the management of study participants enrolled in clinical trials related to the study of trauma, burn, and wound treatments.
$34.78 - $55.92 an hourFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Job title: Senior Research Scientist – Nutrition Research & Clinical Investigator. We are looking for a Senior Nutrition Research & Clinical Investigator passionate about ensuring the sound science of our nutrition products, along with developing relevant and meaningful product and program solutions that address key customer needs in the global nutrition space.
$107,914 - $139,653 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The scope of responsibility for a Research Interventionist is greater than that for a Clinical Research Specialist due to any combination of the following: greater level of independent safety or clinical decision making required; greater level of specialized clinical knowledge required; substantial contribution to areas such as project intervention materials, plans, study design and research papers; and comprehensive consultation role on policies and methodology.
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The Clinical Research Coordinator will perform independently to execute, manage, and coordinate research protocols, as directed by the Clinical Research Manager and/or the Principal Investigator (PI), and/or the Associate Director for the Clinical Research Programs.
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The clinical research coordinator will assume responsibility for study coordination and day-to-day project duties. The Department of Radiology at the Massachusetts General Hospital is recruiting a full-time Clinical Research Coordinator I to join its multidisciplinary research team.
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The Associate Director, Non-Clinical Study Toxicologist will have overall responsibility for leading in vitro and in vivo discovery safety screening efforts enable data-driven safety decisions regarding the advancement of novel molecules proposed for use in therapeutic development programs.
$170,000 - $226,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Our global Clinical Operations colleagues within our PPD® clinical research services provide end-to-end support for clinical trials from study start up to monitoring through to study close out, across commercial and government contracts.
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He or she will perform a preliminary protocol assessment with the Supply Chain Lead (SCL), Clinical Research Pharmacist (CRP) and clinical team members (e.g., clinician, biostatistician) to determine the most effective IRT strategy for clinical customer, investigator site, Global Clinical Supply, and ultimately for the patient.
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The principal investigator within the Craig Dalsimer Division of Adolescent Medicine, PolicyLab, and the Gender and Sexuality Development Program at the Children’s Hospital of Philadelphia is seeking a Research Scientist to assist with a growing portfolio of research on improving health and well-being for transgender and non-binary children and adolescents.
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Finally, they may also be responsible for providing study coordination for investigator-initiated studies, multi-center research studies, and patient-oriented clinical and translational research projects as needed.
$37,220 - $52,661 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Lab work and management: Research laboratories in the Mike Toth Head and Neck Cancer Center study how alterations in cancer genomes impact response to treatment, and how treatment responses can be predicted and tracked.
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It has direct responsibility for implementing a diverse portfolio of research activities for one or more studies which may include multicenter clinical trials (both NIH and industry-sponsored), local investigator-initiated clinical trials, and/or programmatic clinical research activities, such as a clinical database and biorepository.
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Knowledge of clinical research budgeting and the clinical trial life cycle: study start-up through study closure. Disseminates the completed coverage analysis to key stakeholders to expedite clinical research start-up.
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As a Clinical Research Associate I, you will work directly with a Clinical Research Coordinator, Research Program Administrator, Research Nurse, or Principal Investigator to coordinate and/or implement the study.
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clinical research investigator study start up jobs Company: Cedars Sinai
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