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CRCs are responsible for assisting study start-up; recruiting, enrolling, and retaining participants in the study; performing study assessments and follow-ups; data entry and management; and facilitating community outreach and stakeholder engagement.
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The CM will develop and implement discharge plans for those patients identified as needing post acute discharge services or post acute follow up in collaboration with the patient/legal representative, health care team/provider, insurer, and others, including community based organizations, as needed.
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Must be able to ability to proactively improve processes; direct the inspection and calibration of DDC systems and devices to detect abnormal function and follow through with recommended repairs; prepare schematic drawings, sketches, and reports; read ladder diagrams, blueprints, and schematics; and manage work order backlogs and prioritize work.
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Work with PM team and Tenant Engagement Manager to complete tenant surveys as needed and follow-up with actionable items. Ensure all tenant database information in PM systems, or otherwise, is up to date and accurate.
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Under the direction of the clinical leaders, performs radiographic procedures that follow radiological standards in a safe, accurate and timely manner which are necessary to allow the radiologist and/or physician to make a radiological diagnosis.
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Make recommendations to the Year Up STS team to strengthen partnerships for student support services offered on-site and off-site. Make recommendations to Year Up Student Services team, site leadership, and college partners to improve collaborative experiences for the student support services offered on-site and off-site.
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This role will report to a Senior Scientist on the Translational Research team with autonomy owning various stakeholders, projects, and tasks in a dynamic start-up environment while keeping up the pace of Alloy.
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The Clinical Trial Manager, Site Start-up will lead internal process improvements related to study start up activities to ensure clinical trials are executed with high quality standards in compliance with regulatory requirements, GCP, and company SOPs. This role is based in our Waltham, MA headquarters.
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Responsible for external outreach with KOLs and key clinical trial sites to provide feedback on study feasibility and study start up activities. Clinical Trial Initiation Manager will deliver high quality and timely global study start-up.
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Oversee the informed consent process and translation of study required documents and participate in the development of study start up plans. The Clinical Trial Manager, Site Start-up will serve as an expert in study start-up practices by initiating efficient start-up activities and removing obstacles for study teams.
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Develop a Site Initiation Management Plan and coordinate regulatory and ethics committee submissions and perform day to day management of the study start up activities for clinical studies. Provides internal expertise in the early planning of study start-up to ensure proposed CRO timelines and committed milestones are accurate and achievable.
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Manage study start-up planning, and modeling. Reporting to the Director/Senior Director of Clinical Operations, the Clinical Trial Manager, Site Start-up is accountable for leading, directing and overseeing end-to-end start-up, site initiation and site activation in collaboration with key stakeholders across multiple complex studies in a fast-paced environment.
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Responsibilities (including, but not limited to):•Provides key data driven insights to study teams for study, country, and site feasibility along with start-up and enrollment forecasting. Partners with CRO to ensure effective start-up processes, utilizing appropriate technologies, as required, to deliver best in class country and site activation performance.
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The Clinical Trial Manager, Site Start-up role plays a significant contribution to the clinical trial execution and ability to meet the corporate study goals for the Company clinical Clinical Trial Manager, Site Start-up will lead internal process improvements related to study start up activities to ensure clinical trials are executed with high quality standards in compliance with regulatory requirements, GCP, and company SOPs. This role is based in our Waltham, MA headquarters.
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A career at Fidelity within Global Security Operations (GSO) as a Security Representative will equip you with not only a fundamental security skillset that is first in class, but also essential qualifications for any career path you choose to follow.
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follow up jobs Title: team member in Cambridge, MA
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