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The Clinical Research Supervisor reports to the Research Administrator, Clinical Trials Manager, Research Vice Chairs and works directly with Principal Investigators within the Department of Obstetrics, Gynecology and Women's Health on the execution of reproductive health research studies, focusing on protocol development and coordination, supervising research/study assistants, and data cleaning and monitoring.
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Preferred Qualifications:Experience building UI with ComposeExperience with streaming video (DASH or HLS protocol), codecs, and DRMDirect experience mentoring or managing othersRequired Education: Bachelor’s degree in Computer Science, Information Systems, Software Engineering, or comparable field of study, and/or equivalent work experience.
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Maintains databases as per operating procedures and under guidance of database programmer and study coordinator(s). Among the key duties of this position are the following:Works with international sites in data capture, quality assurance/quality control (QA/QC) and regulatory activities during protocol conduct.
$16 an hourPart-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Lead or co-lead development of a trial protocol and other study-related and regulatory documents, case report forms (eCRFs), eCRFs completion guidelines, database lock activities, and medical data review plan.
$196,000 a yearFull-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Submits or partners with a regulatory coordinator to submit study related documents, study protocols and study protocol amendments to the IRB per policy and procedure. Provide ongoing study status updates, respond to questions and may create summary report(s) for distribution to PI, Administrator, Office of Research Affairs, Sponsor and Compliance throughout the conduct of the study.
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Study start up, ensure all protocol requirements are met, ordering of proper supplies, development of vendor relationships, coordinate staffing and proper coverage. Manage and track vital trial metrics and operational objectives for the trial are in conformance to all relevant laws, regulations, GCP guidelines, protocol, and internal SOPs/policies.
Full-timeExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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If applicable, reviews and completes protocol history sheets, flow sheets, study follow-up reports and patient evaluation forms. Educates patients and staff on pharmacological/drug effects and protocol requirements, if applicable.
$156,600ExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Report protocol deviations to PI, sponsor, and IRB as required. Ability to efficiently operate all job-related office equipment (telephone, computer, calculator, fax, copier, study-specific equipment.
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Maintaining a working knowledge of current FDA regulations, ICH-GCP guidelines, all the organizational SOPs, all the guidance documents, and assigned study protocol(s) Conducting and overseeing study subject visits, and all other relevant protocol-required procedures and documenting these in a timely manner.
$76,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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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.
$92,650 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Collaborating cross-functionally in the development of Protocol and related study materials (e.g., ICF documents / amendments); partnering with Clinical Operations on study deliverables.
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As a Clinical Research Associate you will be responsible for a variety of monitoring tasks and you will have a chance to work on clinical studies in different therapeutic indications, ensuring the clinical trial is conducted in compliance with study protocol and procedures, ICH-GCP guidelines and the applicable regulations and SOPs.
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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.
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As the Lead CRC, you will act as the subject matter expert and leader of a clinical trial team to conduct and manage clinical trial(s) from start up through study close out in accordance with the study protocol, GCP, and Eximia Clinical Research’s SOPs.
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This will include method selection, development of study protocol, data collection, and analysis of user behavior / perspectives via qualitative and quantitative methods, as well as creating / communicating research findings, insights, and recommendations to groups of cross-functional stakeholders.
$65 an hourExpandApply NowActive JobUpdated Today
protocol study jobs in New York, NY
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