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Plan and execute experiments based on bioanalytical protocol and in vivo study design. · Qualify ligand binding assay based on bioanalysis protocol, interpret result, and make decision on assay readiness.
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Lead the team to design and coordinate key/priority aspects of epidemiologic Solid Tumor Oncology research programs, including study design, protocol preparation, directing design and preparation of data collection forms and data tabulations, preparing data summaries/reports, publications (e.g. scientific manuscripts, abstracts, posters, internal and external presentations), systematic reviews, and technical reports.
Full-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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The Cognitive Neuropsychology Laboratory (CNL) at the Albert Einstein College of Medicine is comprised of a multidisciplinary team of investigators, post-doctoral fellows, and students using psychophysics, EEG, and MRI to study attention, auditory and visual perception, multisensory processing, and executive function, in typical and clinical populations.
$41.99 - $43.84 an hourFull-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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The Senior/Clinical Trial Manager will have independent oversight of outsourced Clinical Studies including but not limited to: protocol review for operational feasibility and consistency, CRO/vendor feasibility, request for proposal and bid defense process, country/site feasibility, tracking site selection, activation and patient recruitment, management of project timelines, relevant study plans (e.g. monitoring, study operations, quality, communications, etc.
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The role will lead and provide direction to the Clinical Project Team to ensure all trial outputs (from protocol development to Clinical Study Report) are delivered on time, within budget, and with high quality, in adherence to internal SOPs, GCP and applicable regulatory guidelines.
ExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Responsible for Institutional Review Board (IRB) protocol submissions. Serve as a backup for PET/MRI scheduling and completion, as well as neuropsychological test administration and other study procedures.
$58,500 - $70,000 a yearFull-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Closely and liaise with the clinical operations team, clinical study teams, pharmacovigilance, the SVP and stakeholders. Knowledge of clinical trial methodology, regulatory and compliance requirements governing clinical trials, and experience in strategy development and protocol design.
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Adheres to good clinical practice, and complies with regulatory and grant agency requirements, and study protocol; maintains study records and collaborates with the institutional review board as necessary.
$58,540 - $92,650 a yearFull-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Protocol deviation category and other study documents for the project. (c)Develop the protocol, clinical research report, investigator brochure, medical monitor plan. ⚫Familiar with GCP and the SOP of clinical study.
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Prepares for upcoming study visits: research bio-specimen collection order preparation/placement, laboratory and EKG order placement, scheduling of biopsies and scans, interpreter requests, facilitating tumor assessment form completion from the investigator, QOL, AE and ConMed form completion in conjunction with a licensed professional (CRN/APP/MD) and other tasks as needed to support seamless, safe, and compliant clinical research conduct per protocol.
Full-timeExpandApply NowActive JobUpdated 14 days ago - UpvoteDownvoteShare Job
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The Clinical Research Coordinator performs study coordination tasks under the direction of the investigator and works closely with the Senior Research Scientist to ensure overall compliance in the conduct of the study, and adherence to the approved study protocol.
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Review and adhere to sponsor requirements pertaining to study medications for specific study protocol (i.e., integrate sponsor requirements into Frontage procedures; resolve any discrepancies in consultation with Principal Investigator; Director, CRC Operations and sponsor if necessary.
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Provide oversight of and insights into trial activities (e.g., trends in protocol compliance, enrollment, monitoring deviations, data quality) to principal investigators and support staff, and study sponsor management and leadership staff, including Institutional Review Boards/Ethics Committees/Research Ethics Boards, Contract, and Training, developing process improvements.
Full-timeExpandApply NowActive JobUpdated 30 days ago - UpvoteDownvoteShare Job
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The Biostatistician II is responsible for providing statistical support, including study design, sample size and protocol development in support of clinical projects. Writes statistical text for study reports and clinical publications.
ExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.
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protocol study jobs in Jersey City, NJ
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