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Assist with miscellaneous research released task: data entry, preparing paperwork for participant visits, filing paperwork related to participant visits, backing up computer files following participant visits, organizing files, posting flyers, escorting participants from one location to another (e.g., from the Clinical and Translational Research Center to CCN for neuroimaging.
$16.5 - $27 an hourInternExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Contribute to the preparation of clinical protocols, amendments, informed consent forms, study manuals and guides, electronic case report forms, and any other clinical research related documents.
$155,000 - $165,000 a yearFull-timeExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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Minimum of 5 years of experience in Clinical QA, with a focus on auditing clinical trial sites (Investigators) during various phases of a clinical research study (as applicable), vendors and contract research organizations.
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Facilitating collaborations in Neurosurgery, Indiana Spinal Cord and Brain Injury Research Group (ISCBIRG) and Stark Neuroscience among investigators and between clinical and pre-clinical faculty to establish new research areas, particularly within areas of established strengths.
ExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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The interns will be responsible for screening and identifying potential candidates for enrollment in current clinical trials, assist the research staff in the enrollment process for each study, and complete data collection and data entry as directed.
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Serve as a subject matter expert on tissue collection practices and participate in internal research team discussions regarding study design and implementation. Build, manage and train a team of necropsy prosectors for execution of non-clinical necropsies to support the Gene Therapy, Gene Editing, and RNA programs.
$83,600 - $104,500Full-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Position-Specific Responsibilities Under the supervision of Dr. Jeffrey Schnipper of the BWH Division of General Internal Medicine, the Clinical Research Assistant works directly with enrolled subjects as an essential research team member, tasked with the direct observation of in-hospital pharmacist workflow for a prospective pre-post mixed methods hybrid type 2 effectiveness-implementation study.
TemporaryExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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Maintain protocol compliance on all clinical trials/studies according to the International Conference on Harmonization-Good Clinical Practice (ICH-GCP), local regulations, and study protocol.
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The CRC / Clinical Research Coordinator coordinates neurology/stroke-focused study protocols for the research department. Clinical trials involve enrolling patients in fast-paced, cutting-edge, acute care stroke and traumatic brain injury studies in collaboration with physician leaders in stroke, neurology and neurosurgery.
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Assist Clinical Scientist, Study Responsible Scientist (SRS), &/or Study Responsible Physician (SRP) in various clinical research assigned Immunology Development clinical trials.
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Coordinates the implementation, both internally and externally, of sponsored clinical research studies. Working independently and under very general supervision, provides support to clinical research studies.
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The Research Nurse Coordinator is a primary resource for study protocol conduct acting as a liaison between the University of Massachusetts Medical School (UMMS), clinical partners (ex.
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Clinical skills that may be required include, but not limited to: patient assessment for adverse events and assistance with, or completion of, study related procedures as detailed in the research protocol (ex: injections, phlebotomy, or infusions), within the applicable state scope of practice.
$44Full-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Supports clinical research associates and medical doctors in clinical protocol development. Job Category: Research & DevelopmentReports to: VP of Clinical DevelopmentJob Type: Full timeContract or Direct HireLocation: REMOTE BasedPay Rate: Depends on ExperienceCompany Type: Pharma, 600 Employees globally with HQ in Boston.
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Required Education and Experience:Bachelor's degree in life science, health professions or related field and four years of directly related clinical research coordinator experience. Primary responsibilities include the coordination of study enrollment; oversight of study protocols; and submission of research activities per IRB regulations.
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