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Assisting with study start up activities including investigator initiated studies. The person will support the Renal Physician Investigators in clinical research ranging from observational trials to investigational drug/investigational devices, including investigator-initiated, government funded, and industry-sponsored trials.
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This position is responsible for study coordination for investigator-initiated studies, multi-center research studies, and patient-oriented clinical and translational research projects.
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The CRU Regulatory Affairs Office seeks a full-time Regulatory Affairs Veeva Quality Assurance Specialist to participate in the review and migration of Phase I-V clinical trial investigator site files to the Veeva SiteVault platform.
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JOB DESCRIPTION for Financial Investigator II or III. Financial Investigator III. Financial Investigator II. Conducts research, data analysis and interviews to develop information necessary for the referral of suspicious activities to licensing boards and/or law enforcement agencies.
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The position's role focuses on provision of comprehensive statistical support, specifically related to design and implementation of studies, collection and management of study data, patient safety monitoring, statistical data analysis, and interpretation of statistical data for preclinical studies, clinical trials, retrospective studies, epidemiological, and bioinformatics-related research, and summarization and reporting of study results for professional conferences and publication.
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A Brief OverviewThe principal investigator within the Craig Dalsimer Division of Adolescent Medicine, PolicyLab, and the Gender and Sexuality Development Program at the Children’s Hospital of Philadelphia is seeking a Research Scientist to assist with a growing portfolio of research on improving health and well-being for transgender and non-binary children and adolescents.
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Supports study start-up/conduct/close-out activities as applicable in collaboration with clinical operations and CRO. Collaborates with study team members (including Clinical Operations, Drug Safety, Regulatory Affairs, Precision Medicine, Project Management) to ensure that key milestones are met on time and with high quality.
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The Executive Director must prioritize donor discovery, engagement, and giving at all levels and particularly at the major gifts level, while ensuring appropriate coordination with senior executive leaders of the Hospital, Research Institute, Foundation, senior clinical and research leaders, board and other high-level volunteers, and frontline fundraising colleagues dedicated to specific clinical areas to support specialized work.
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A dedicated position as a surveillance investigator. Hold a valid Private Investigator license - where applicable. Capability to start work as early as 5:00 am daily, with occasional evening shifts.
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We need an energetic recent graduate looking to start a career in a fast-paced environment with a company at the forefront of hi-tech complex manufacturing to travel up to 75% of time within North America.
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The In-Vivo Program Manager will play an integral part in overseeing vendor relationships related to clinical research into immunological pharmaceutical products. Participate in design of experiment (DOE) of clinical studies related to immunological pharmaceutical research.
$125,000 - $150,000 a yearFull-timeExpandApply NowActive JobUpdated 15 days ago - UpvoteDownvoteShare Job
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Personal statements summarizing teaching experience, clinical and research interests, and contributions to diversity are strongly encouraged. Temple Health is one of Philadelphia's leading academic medical centers, with 20 clinical departments; 8 Basic Science Departments; 13 Research Center (all of which are engaged in patient care education and research) and more than 1,000 physicians and scientists sharing the mission of bringing innovative treatments to patients.
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The Associate Scientist, Process Development will be responsible for refinement, development, characterization, and assist transfer of product candidates through to Cabaletta's cell therapy CMO. This position will work very closely with internal stakeholders (MSAT, AD, Pre-clinical, QA, CMC, Regulatory) , and require up to 10% domestic travel or occasional weekend and overtime work.
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Clinical Research Nurse C ResponsibilitiesWork in collaboration with Research Team Leaders and Principal Investigators with initiating study procedures for new IITs and industry-sponsored clinical trials.
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You will be on the clinical frontlines supporting our members, and you'll gain broad exposure to operations in a rapidly growing health-tech startup. We’re building the world’s most advanced healthcare platform from the ground up, combining hardware, software and doctors under one roof.
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clinical research investigator study start up jobs Company: Cedars Sinai in Philadelphia, PA
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