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Our research aims to improve quality of life, well-being, symptom and pain management, and reduce caregiver burden:For example, a Clinical Research Coordinator to support a large multi-site clinical trial study that focuses on the comparison of care delivery models to support older adults with complex healthcare needs.
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Play a pivotal role in hotel sales efforts including calling on top ten accounts meeting clients hosting luncheons and receptions and meeting with on-site contacts on a daily weekly and monthly basis.
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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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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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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. 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.
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Serves as a point of escalation for study teams and CROs for country and site activation issues. 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 programs. Responsible for data driven assessment of country and site scenario planning, patient enrollment assumptions and start-up data.
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Partners with Clinical Operations, Medical Affairs/local country offices to obtain local insights into country and site selection. Prepare, distribute, and collect site-specific essential document packages.
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Non-essential functions:Assist Conference Services Department as required, particularly during large group movementsMentor and develop Administrative staff for future career growthAssist with all guest inquires within the Sales, Marketing and Conference Services Department, including assistance with high telephone volume and walk-in site inspections.
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The Deputy Chief of Security regularly meets with Facility Managers to discuss site-specific security needs and to foster operational collaboration and regularly reports to the Chief of Security & Emergency Preparedness regarding current security trends or concerns and makes recommendations to advance the Agency’s security program.
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The Service Desk Manager manages the Support Analysts, Support Consultants and student employees staffing the Service Desk. This is primarily an on-site position. HDI Support Center Manager certification and HDI Desktop Support Manager certification.
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On-site or regional Fertility, Maternal-Fetal Medicine and other women’s health subspecialty services. On-site laboratory, radiologic and pharmacy services. BID Plymouth, Lowell General Hospital, Mount Auburn Hospital, Newton Wellesley Hospital, South Shore Hospital and Winchester Hospital.
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REPORTS TO: Position reports to the Site Coordinator, who works in close collaboration with the Director of Extended School Year and Expanded Learning in the Office of Special Education. Provide students, families, site coordinators, and program staff with relevant and timely data, including monitoring and reporting student's progress to prevent regression as outlined in the program.
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The Associate Director is responsible for the academic rigor of all programs and academic policies at BU Study Abroad sites, working with the directors and faculty on site to assess, train, advise on academic matters and update them on BU (and BUSA) academic policies and procedures.
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site job Company: Mspca Angell in Boston, Needham, Massachusetts
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