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ATEC Spine has an exciting opportunity for a Director of Clinical Research & Strategy as a member of the Scientific Affairs team located in Carlsbad, California. The Clinical Research function, as a sub-function of Scientific Affairs, includes planning, coordinating, and overseeing the successful execution of preclinical and clinical research studies and large-scale data collection efforts in partnership with our surgical practice partners.
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Supporting the Director of Global Scientific Affairs, in conjunction with the Sr. Manager and Project Manager in Global Scientific Affairs, with KOL management as it relates to investigator-sponsored studies (ISS) and/or collaborative research studies (CRS.
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This position is housed in the Clinical Research Support Office (CRSO), a centralized clinical trial management office in the UCSF Helen Diller Family Comprehensive Cancer Center (HDFCCC), which provides project management and clinical research coordinator staff, and regulatory services for oncology related clinical trials.
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Cultivate engagements between Danaher and biopharma key opinion leaders (KOLs) in neurology and related disease areas; possess in depth knowledge of biopharma drug pipelines in neurology and anticipate the diagnostic needs of pharma (from Research Use Only (RUO) to Clinical Trial Assay (CTA) to In Vitro Diagnostics (IVD) inclusive of Companion Diagnostics (CDx) and Lab Developed Tests (LDTs.
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Proven track record of success in neurodegenerative disease human clinical trial research and/or clinical management of patients with Alzheimer's Disease and Dementia a plus. Support Danaher Diagnostic Operating Company Medical and Scientific Affairs and Government Affairs organizations on their strategy so that it maximizes patient impact at scale.
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Lead the execution of global CMC regulatory plans, including overseeing the submission and approval process in close partnership with other functions in Research and Development, Regulatory Affairs, and Clinical Development.
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Strategic Analysis is seeking a versatile, skilled Legislative Affairs Specialist to support the Defense Advanced Research Projects Agency (DARPA) Director's Office. Draft, track, and manage DoD/legislative affairs reporting requirements as they pertain to DARPA and DARPA requirements/responsibilities.
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Leads the execution of global CMC regulatory plans, including overseeing the submission preparation process in close partnership with other functions in PDM, Regulatory Affairs, and Clinical Development.
$237,660 - $307,560Full-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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This position is part of Clinical Affairs team and will be hybrid to Sunnyvale, CA. The senior clinical research scientist will work on advanced, complex projects requiring state of the art knowledge in oncology and/or infectious disease molecular diagnostics.
$103,000 - $142,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The Field HEOR Sr. Director or Director (FHD) position will lead clinical, health economics and outcomes research communications with population health decision-makers to ensure effective delivery of value stories and support for BeiGene products.
$187,800 - $257,800 a yearFull-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Collaborate with commercial, market access, and medical affairs to set the agenda for and design clinical oncology research initiatives including collaborating with external KOLs to define publication strategies.
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1 or More Years’ experience including medical & scientific affairs, clinical practice, research, academic or US managed markets preferred. 5 or More Years’ experience including medical & scientific affairs, clinical practice, research, academic or US managed markets preferred.
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Identifying and appropriately facilitating engagement of qualified 1) investigators and study committee members for DSI clinical research programs, 2) investigator-initiated research study proposals, 3) speakers for DSI Brand Speaker programs, 4) advisors for DSI scientific, clinical and marketing advisory boards.
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Previous experience in Oncology, clinical research and medical education preferred. Daiichi Sankyo, Inc. (DSI) is currently seeking a Medical Science Liaison (MSL) to join the Field Medical Affairs Team. The MSL develops on-going professional relationships with national and regional healthcare opinion leaders and other healthcare professionals to provide medical and scientific support for Daiichi Sankyo, Inc. (DSI) initiatives in selected therapeutic areas.
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Enrolled in a Masters, PhD, or Graduate program related to digital health policy, regulation, user research and/or bioethics. As The Focus Of This Internship, We Would Like To Study The Potential For How Generative AI Can Be Used In The Drug Development Lifecycle To Accelerate The Approach To Areas Such As Regulatory Filings, Generation Of Real World Evidence, Clinical Trial Documentation And Audits.
$6,290 - $12,170 a monthInternExpandApply NowActive JobUpdated 12 days ago
clinical research affairs jobs Title: director Company: Biophase
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