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SES Electrical LLC (SEL), a subsidiary of Bristol Bay Construction Holdings LLC (BBCH), is currently seeking a highly skilled professional to join their team as a Quality Control Manager/Site Safety & Health Officer.
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The Site Safety Manager will be responsible for ensuring all aspects of safety and accuracy are maintained on all projects. The manager will also maintain all required safety and quality documentation for the project controls in accordance with the corporate safety standards and project specifications.
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The Assistant Site Manager, Family Emergency Shelters, supports the daily operations of a shelter operating at a hotel location with coordination of scheduling, transportation coordination, the prioritization and direction of tasks for case management, housing, employment navigation, and nursing.
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New York City (Hybrid On-Site): $165,100 - $188,500 for Prin Assoc, Cyber TechnicalSan Francisco, California (Hybrid On-Site): $174,900 - $199,700 for Prin Assoc, Cyber Technical. Capital One does not provide, endorse nor guarantee and is not liable for third-party products, services, educational tools or other information available through this site.
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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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Leads end-to-end event management and on-site execution, including documentation, catering orders, internal and external communications, and set-up, event, and strike supervision. Promotes the revenue goals of the Development department to meet or exceed sales goal by developing fiscal year sales plans; proactively attracts new event sales leads, addresses inquiries, hosts site visits, and contracts clients/events.
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Perform all department manager performance appraisals according to Aimbridge Hospitality S.O.P.'s and ensure that managers are in compliance with the standards in their administration of performance appraisals to their staff.
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At the newly designed Leiden Center 1 site in Boston Seaport and other greater Boston locations, Vertex envisions the growth of CGT pipelines research, development, and clinical manufacturing for emerging therapeutic modalities with the potential to treat and even cure Type I Diabetes.
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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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Assist with all guest inquires within the Sales, Marketing and Conference Services Department, including assistance with high telephone volume and walk-in site inspections. Review all function space with banquet manager and when required head house attendant.
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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. 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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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.
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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. Serves as a point of escalation for study teams and CROs for country and site activation issues.
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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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site job Title: manager in Lynn, MA
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