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Works closely with the EMS vendor and ERCOT GMS development teams to reproduce defects and test the fixes. Participates in planning and evaluating the impact of system modifications and maintenance activities to ERCOT grid operations.
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He/She 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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DescriptionThe Technology Chief Financial Officer, ('Tech CFO ') is responsible for financial leadership of Humana's global Tech operations, including strategy and execution from new project prioritization and planning to ongoi.
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O Participate in strategic study start-up planning in collaboration with GCO, C&G, and RTAEs including early site assessment, feasibility, and use of simplified contract and budget templates to accelerate rate of site activations.
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Work closely with functional partners (Data Management, Biostatistics, Regulatory, GCO, QMMC, GMS) to ensure an integrated and strategic approach to flawless execution and systematic oversight of study protocol(s) in late development in close collaboration with key functional stakeholders.
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O Working closely with the colleague study responsible physicians and clinical project scientists in collaboration with GCO and GMS to ensure comprehensive medical monitoring, thorough and timely responses to address site issues and eligibility questions, and detailed, real time review of serious adverse events and deaths.
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Janssen Research & Development, LLC discovers and develops innovative medical solutions to address important unmet medical needs in oncology, immunology, neuroscience, infectious diseases and vaccines, and cardiovascular and metabolic diseases.
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O Work with GCO to provide oversight of CRO/study vendors' performance as it relates to study start-up and conduct. Janssen Research and Development, L.L.C., a member of Johnson & Johnson's Family of Companies, is recruiting for a Medical Director/Senior Medical Director, Clinical Research - Solid Tumor.
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At the Janssen Pharmaceutical Companies of Johnson & Johnson, what matters most is helping people live full and healthy lives. Organization Janssen Research & Development, LLC (6084) May interact with medical consultants in concert with senior clinical staff, in conducting IDMC and Investigator meetings as well as Advisory Boards.
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May review/co-author medical publications emerging from clinical trial results. The preferred locations for this position are Raritan, NJ or Spring House, PA; however, we will also consider remote work within the U.S.
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Collect and compile giving opportunities and nonprofit information to be easily shared across the Development and Donor Services (DDS) department, utilizing the Grants Management System (GMS) system and other knowledge management tools.
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A minimum of 2 years of oncology clinical research experience in clinical development within pharmaceutical industry or equivalent experience in academic or large regional hospital is required. Experience in protocol development, medical review, oversight of study conduct, running trials, data quality and safety are strongly preferred.
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Knowledge of Good Clinical Practices and regulatory requirements for the conduct of high quality oncology clinical trials is required. May be asked to assess and plan for external clinical research opportunities in collaboration with Clinical Leader and BD.
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The successful person in this role will provide mentoring and support to the clinical project scientists on the team and will work with PMO, Finance, and the Clinical Leader to assure appropriate resourcing of clinical studies.
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The Director / Sr. Director, Clinical Development-Oncology will contribute to the development and oversee the execution of oncology clinical research studies, ensuring consistency and quality, across the assigned development program.
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