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Collect study specimens according to protocol. The Research Coordinator will be responsible for recruiting subjects, scheduling subject appointments, interviewing adults and children using structured psychiatric interviews and neuropsychological tests, assisting in performing MRI scans, processing financial forms and administering informed consent to study participants as well as ensuring quality of data collection and data analysis.
$27.4 - $31.25 an hourExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Top daily responsibilities:¿ Scoping research questions and getting alignment from cross functional team¿ Planning research activities¿ Designing study protocol¿ Creating highlight videos/screenshots¿ Analyzing and interpreting both qualitative and quantitative data¿ Creating findings and recommendation reports from user studies.
ExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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This individual will collaborate closely with the cross-functional teams on protocol development, study execution, be responsible for data analysis and interpretation of results, and work closely with Data Management and Statistical Programming resources to achieve all Biometric deliverables and activities at CROs. Additional analysis support of non-clinical / biomarker /CMC data and derive insight to contribute to Ascendis' scientific research may be requested.
ExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Responsibilities include working collaboratively with the research team and clinical teams to help manage participant screenings, consent process, study procedures, IRB protocol compliance, and general communication with both internal and external stakeholders.
Full-timeExpandApply NowActive JobUpdated 12 days ago - UpvoteDownvoteShare Job
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Participates in the functional review of study protocol and other study related documents such as clinical sample management plan, study communication plan, or presentations for Investigator and/or Study Kick-Off meeting.
ExpandApply NowActive JobUpdated 12 days ago - UpvoteDownvoteShare Job
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Package and ship samples for processing per the research protocol;Provide general clerical assistance when needed, e.g. answer phones, greet subjects; photocopy study forms. Duties include assisting with recruiting subjects, helping with using rTMS machine to stimulate designated area of the brain in the RCT after being trained by a professional, entering data in study databases, administering neuropsychological and neurophysiological testing and assisting with data analysis under the direct supervision by the Principal Investigator - Dr. Maheen Adamson.
ExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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Serves as the study level biostatistician including participating in study design and protocol review discussion, conducting sample size calculations, developing statistical analysis plan, data presentation plan and DMC charter, reviewing study documents (e.g. CRFs, ADaM specifications, statistical outputs, and etc.
Full-timeExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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As our Clinical Trial Manager (CTM), you’ll be accountable for the day-to-day study management and successful delivery of one or more clinical trials in accordance with the protocol, Arcellx SOPs and good clinical practices (GCP) and applicable regulations.
$125,000 - $170,000 a yearExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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Study design and protocol development, including sample size estimation, formulation of statistical hypotheses and testing strategy, and statistical methods. Provide statistical insight into the interpretation and discussion of results for sections for the clinical study report (CSR), the ISE, ISE, publications, and business decisions.
$220,000 - $260,000 a yearFull-timeExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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Provide scientific expertise for selection of investigator and vendors Train BeiGene colleagues, CRO staff, and study site staff on the therapeutic area, molecule, and/or clinical protocol.
$168,800 - $228,800 a yearFull-timeExpandApply NowActive JobUpdated 20 days ago - UpvoteDownvoteShare Job
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Plan observational studies and draft protocol synopsis (or protocol concept sheet). Draft and review observational study analysis specifications, including statistical analysis plans (SAPs.
ExpandApply NowActive JobUpdated 20 days ago - UpvoteDownvoteShare Job
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Knowledge of full cycle clinical study management, from start-up to close-out, and has shown ability to effectively apply this knowledge to achieve targeted study outcomes. You may manage certain components of clinical studies and act as a member of the study team.
Full-timeExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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These activities include, but are not limited to, study protocol preparation, additional study or investigator documentation, contributions to data analysis plans, study reporting, and clinical development inputs into regulatory documentation, publications and scientific presentations.
$295,290 - $382,140Full-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Job Title: Study Epidemiologist HIV/ Sr Manager Drug Safety & Public Health. Review analysis outputs for quality, including study analysis, ad hoc analysis, analysis to support conference or publications.
ExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Ensure study team members and vendors are trained on protocol, relevant studydocuments, and key decisions at study start-up and throughout the duration of thestudy. Participation in large multi-center and/or global trials, investigational site andCRO management, data collection, and study protocol compliance.
ExpandApply NowActive JobUpdated 4 days ago
protocol study jobs in Menlo Park, CA
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