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The Activities Coordinator will be responsible for the overall recreational therapy component of the Safe Haven Programs following the Housing First and Harm Reduction models. Conduct in-house recreational activities on a weekly basis, such as movie night, bingo, cards, music appreciation or other such pastimes.
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Schedule: Mon-Fri, 8am-4pm Salary: $21.50 / hour As a Day Program Activities Assistant, your direct care and instruction will support adults with intellectual disabilities, developmental disabilities or behavioral challenges to achieve goals, overcome barriers, and build life skills in a Day Program or Day Habilitation setting.
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Delivers appropriate education/skills/recreational/activity in groups and individual activity modules/plans as assigned by the Group Therapy Coordinator, which represent current interests and needs of patients, pertaining to nature of the unit” Provides feedback on an ongoing basis to the Group Therapy Coordinator on patient response to, or progress with, activities.
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Proactively identify and resolve client issues Engage in high level trust administration; oversee all administration activities Document interpretation Oversee risk management activities Identify at risk clients; proactively resolve issues / meet with at-risk clients as needed to drive retention Requirements: Bachelor’s Degree and a minimum of 5 years of trust administration and estate planning experience, preferred.
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There will be daily and weekly scheduled activities such as gym games, swim instruction, roller skating, along with dance, music, art, and seasonal, intramural and competitive sports. These activities can include, but are not limited to, roller skating, cooperative games, skill building activities and skills development.
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Capabilities to evaluate a broad range of an institutions’ practices in capital markets risk dimensions and businesses, the risk management techniques in hedging market risk and credit and collateral management, along with independent risk and product and trade control functions applied across front, middle and back-office activities.
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When not engaged in research management activities within the divisions, the Sr. Grant Administrator will provide support for DOM central administration activities as detailed below. As a consultant, he/she will play a key role in the coordination of research activities including special projects, oversight of complex programs or filling short-term vacancies.
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Assists the HSE Department in managing the overall corporate safety program by conducting, tracking and reporting on accident/incident, near miss reports, audits, engagement activities, observations, orientations, trainings and other related safety activities, as well as recordkeeping of related documents.
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Collaborates with the City’s Infrastructure & Asset Management Department, Public Works Department, Parking Department, Fire Department, Police Department and others around capital projects, construction management, operations & maintenance activities (including preparation, implementation and evaluation of Standard Operating Procedures), traffic calming interventions, bike / pedestrian facilities and signal operations.
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Requires excellent interpersonal and management skills, with facility to interact professionally at all levels and plan and initiate new activities. Reporting to and working closely with the Assistant Director, Research Administration, the Sr. Grant Administrator will provide expert research administration support to the 21 divisions within the Department of Medicine (DOM.
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Oversee the development of upstream process development activities (fermentation, microbial strain, cell culture, etc.) SME for upstream drug substance activities for IND filings and clinical development.
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Identifies and supports the DSPV team with document management activities (e.g., electronic Trial Master File, Veeva), including maintaining electronic files internally, and collaborate cross- functionally with Blueprint teams, CRO’s and vendors.
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Oversee release activities for Drug Substance Intermediates (DSI) including batch record review/release activities. The Associate Director, Quality Assurance (QA) Operations role will be the QA technical lead on a selection of external manufacturing and testing project teams and responsible to develop, establish, and maintain Quality Systems, Procedures, Policies and Metrics that support those external manufacturing activities in conjunction with the Director of QA Operations.
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Reporting to the Associate Director, Drug Safety and Pharmacovigilance Compliance and Operations, you will play a pivotal role in drug safety activities, supporting records management and compliance across the clinical development and marketing programs.
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The Pharmacovigilance Scientist (PVS) will serve as a core member of the safety team and is responsible for performing proactive pharmacovigilance activities on a product, or group of products in a therapeutic area or franchise, in partnership with the Global Safety Officer (GSO) to evaluate safety data and signals for both marketed productsand products in clinical development.
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activities job in Newton, MA
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