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Informs investigators and study staff of institutional policies and procedures that support protocol compliance, patient safety and clinical operation's efficiencies. Supports investigators and study teams in adverse event assessments and documents appropriately for protocol required data entry.
ExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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Study Start up: Assist with protocol development, sample size calculation, protocol and case report form (CRF) review. Communicate with clients regarding study protocol or statistical analysis issues as they arise.
$122,800 - $233,400 a yearFull-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Ensuring clinical trial management from FPFV to study close out with strict adherence to study protocol, adherence to all other relevant study manuals, study documents, ICH-GCP Guidelines, FDA Regulations, and ALCOC standards, organizational SOPs and guidance documents.
ExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Clinical Research Budget Analyst II reviews the Medicare coverage analysis based on available study documents, such as protocol, proposed budget, and informed consent, and captures all clinical costs and investigators and study team efforts required to carry out the study, as well as costs for ancillary services.
$69ExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Participate in study-related meetings, including investigator meetings, protocol training sessions, and data review meetings. Lead study design, protocol development, and implementation in collaboration with cross-functional teams.
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Main responsibilities include, but are not limited to, the review of New Study routing forms and essential study start-up documents, the itemized cost analysis and interpretation of clinical protocols into budgets milestones, provide accurate patient cost descriptions for the ICF to be submitted to the IRB, and update budget, milestones, and ICF information as necessary per contract/protocol amendments.
RemoteExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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The Clinical Research Budgets Analyst will be responsible for the timely and accurate preparation and maintenance of budget templates for sponsored clinical trials, including the comparative review against budgets offered by study sponsors and the set-up of study payments milestones in the Clinical Trial Management System.
RemoteExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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The Clinical Research Assistant will work closely with the Center for Interventional Immunology study team to recruit and enroll participants, with and without autoimmune disease, conduct study visits and maintain study records in accordance with specified protocol and procedures for the Translational Research Program Immune Mediated Disease Registry and Repository.
$29.27ExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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As part of a study team, assist with developing and carrying out recruitment strategies. Arrange, conduct and record study visits with participants to collect data and obtain biologic samples following strict protocols and processes.
$20 - $27.74 an hourFull-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Experience using various data collection tools such as administering health questionnaires and phone surveys is preferable. BRI is a world-renowned independent nonprofit research institute affiliated with Virginia Mason Franciscan Health and based in Seattle.
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Clinical Research Budget Analyst II also communicates with other center support services to ensure the harmonization of study documents. Clinical Research Budget Analyst II is responsible for the development and negotiation of budgets for clinical trials and studies regardless of funding source that includes industry sponsors, grants, awards, fellowships, cooperatives, etc.
$44.46 - $66.69 an hourFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Substantial clinical study protocol experience, as lead author, required. Under minimal supervision, the Medical Writer will critically evaluate, analyze, and interpret the medical literature to select primary resource materials for adequate study design, statistical significance, scientific rigor and absence of bias.
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Be compliant with infection control procedures and environmental safety protocol within a facility. + Build a strong physical therapy program+ Enhance clinical expertise, professional and management skills through interaction with managers, therapists and other professional staff, self-study, and other continuing education activities.
$42.93 an hourFull-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Prepare and finalize clinical and/or regulatory documents such as, but not limited to, nonclinical and clinical study protocols, protocol amendments, Investigator's Brochures, regulatory briefing documents, health authority responses, IND summaries (i.e., Module 2), nonclinical and clinical study reports, charters, statistical analysis plans and pediatric documents.
ExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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The Budget Analyst Associate will have overall responsibility for creation of study budgets based on detailed knowledge of the study protocol requirements, additional guidance from the sponsor, and input from assigned key staff.
RemoteExpandApply NowActive JobUpdated 9 days ago
protocol study jobs in Seattle, WA
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