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You will be responsible for providing, scientific leadership, and collaborative working environment to advance the drug candidates from IND through Phase IV. In addition, this position will collaborate with cross-functional stakeholders including in vitro & In vivo pharmacology, clinical biomarkers, DMPK, clinical development and operations, regulatory, CMC, and medical affairs.
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Serve as a leader supporting the overall CPP and/or translational medicine organizational objectives Stay current with scientific advancements and regulatory trends in clinical pharmacology and Pharmacometrics, and apply the knowledge to advance drug discovery and development for the organization; Publish in peer reviewed journals.
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Essential CRC duties include coordinating IRB submissions, recruiting study participants, obtaining informed consent, interacting with youth, young adults and parents related to research projects, scheduling and conducting study procedures, collecting and recording study data, organizing participant payments, maintaining study records, participating in data collection and analysis, and the preparation of scientific presentations, manuscripts, reports, and grants.
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Anne E. Kazak, Ph. D., ABPP is the enterprise director, Melissa A. Alderfer, PhD is the Center Director in Delaware and Susana Patton, PhD is the Center Director in Florida. Minimum of a bachelor's degree in psychology, pre-med, public health, or related.
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Situated in Wilmington, DE, the Director of Marketing for Respiratory Biologics plays a pivotal role in leveraging our scientific capabilities to make a positive impact on the lives of patients.
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The Facilities Coordinator will be seconded from the University of Delaware to the Delaware Innovation Space and be on the leadership team of the Delaware Innovation Space and will receive day to day guidance from the Operations Director of DISI and overall strategic guidance from the CEO/President of DISI as well as administratively from MariEileene Keane for UD specific matters.
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Review independent medical education grant and investigator sponsored trial proposals for strategic and scientific quality. The incumbent will drive the delivery of high quality scientific, medical and strategic communications and evidence generation strategies for the product globally.
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The successful candidate should possess a scientific background and will have an understanding of the unique aspects of cell therapy. Job Summary The Senior Manager, Regulatory Affairs position will support the Regulatory Affairs (RA) Director to help define the regulatory strategy for our innovative next-generation technology for cellular therapy.
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Nichino America’s Regulatory and Scientific Affairs Managers report to the department Director and are responsible for hands on coordination and execution of all federal and state regulatory activities for their assigned crop protection active ingredients and products.
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As a Sr. Medical Director, you will be a member of the Core Medical Team (CMT), a board-certified physician with significant experience in the cardiovascular, renal and metabolic (CVRM) disease area.
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As an Associate Director, Internal Communications, you'll play a pivotal role in channeling our scientific capabilities to make a positive impact on changing patients’ lives. And as you take your career in new directions and to even greater heights you'll be rewarded for your successes.
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