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Oversee vivarium operations and technical in vivo study support at all Vertex R&D sites through management of local technical teams. Provides direction for laboratory and/or vivarium safety both at a site level and globally and performs veterinary reviews of new animal use protocols and study protocols.
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The candidate will serve as a full-time Clinical Research Coordinator (CRC) in the Mass General Early Brain Development Initiative (EBDI), and will report to Dr. Joshua Roffman, director of EBDI, and Dr. Alysa Doyle, director of research at the MGH Learning and Emotional Assessment Program.
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Have a minimum of six months (one year preferred) experience working with school-age childrenExperience with Christian Education Programs for school age children such as Sunday School or Vacation Bible Study preferred Must be able to plan, prepare and implement day-to-day activities.
$20 - $23Full-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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The Senior Research Regulatory Coordinator (RC) works under the direction of the CCI Executive Director, Research Operations Director and Principal Investigator(s) to complete the regulatory requirements of clinical research projects.
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Leading FEMA MIP deliverable compilation and review within a flood risk study lifecycle. Independently lead and coordinate tasks within a Risk MAP flood study lifecycle, such as basemap, terrain, FIRM database development, floodplain mapping, preliminary issuance, and post-preliminary processing through map effective, and delegate tasks to multiple supporting staff across diverse geographies.
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PRINCIPAL DUTIES AND RESPONSIBILITIESStudy Start-up Responsibilities include: Draft/finalize Data Management Plan (DMP)Develop study-specific STATA code to format and manipulate imaging datasets according to the DMP and needs of each study.
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The individual hired for this position will receive general direction from the Senior Project Manager for Clinical Research and the Vice Chief for Research and will work as part of a team of clinical research coordinators to ensure successful study start-up, enrollment and close-out in compliance with MGH, Partners, NIH and FDA regulations and guidelines.
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Assists with Institutional Review Board (IRB) requirements for each study including meeting institutional educational requirements, submitting documents for review such as amendments, adverse event reporting and annual reviews.
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Aquatics Director - Charles River YMCA (Needham, MA) Under the supervision of the Branch Director of Operations, the Aquatics Director is responsible for the supervision and management of all facets of the Aquatics Department at the Branch.
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May develop Standard Operating Procedures (SOPs) and Work Instructions (WIs) as directed by the Senior Director CMC Regulatory Affairs. Prior pharmaceutical industry experience and a minimum of 8 years in CMC Regulatory Affairs for Associate Director.
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The Purchasing Manager role will report to the Purchasing Director to ensure Procure-to-Pay and supplier onboarding practices are being carried out in alignment with the vision, goals, and direction of our Procurement leaders.
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Job Description: Director, Quant Data Engineering The Role The Asset Management Quant Research Engineering team is looking for a Director of Data Engineering who wishes to take on the challenge of building a world-class data operation.
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The director will partner broadly with campus constituents such as but not limited to Development/Alumni Relations, LGBTQIA+ Center for Faculty & Staff, Residence Life/Housing, Student Activities, Howard Thurman Center for Common Ground, Student Health Services, Community & Inclusion, Government/Community Affairs, the Newbury Center, International Students and Scholars Office, and Athletics.
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This person will work closely with the clinical project scientist team and Clinical Leader in Late Development, in collaboration with other functional disciplines, including GCO, Data Management, Statistics, Regulatory, QMMC, and GMS to ensure flawless and integrated execution of study start-up planning, oversight, and reporting of clinical studies in Oncology.
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Core Responsibilities - Accounts Receivable/Payable: Regularly review contracts/budgets, create/maintain study calendars and manually gather data from MGH Cardiology study teamsEnsure timely clinical trials invoicing to industry sponsors which matches protocol driven procedures with patient accruals/visits to ensure appropriate invoicing and reimbursement.
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study director jobs Company: Genoskin in Revere, MA
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