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Position Description:The Clinical Research Coordinator I will be aiding the Research Team and Principal Investigator (Director of Adolescent HIV services and Co-Director of the GSDP) in the coordination of clinical, behavioral, policy and community-engaged research to improve health outcomes of adolescents and young adults.
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Full Stack Development: Lead the design, development, and maintenance of web applications from concept to production.
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In addition to the responsibilities above, the Clinical Research Coordinator B will assist the regulatory specialist in preparing for all local and Central Institutional Review Board (IRB) documentation through the IRB, including submissions, continuing reviews, amendments, modifications, and adverse event reporting.
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What You Will Do: The ideal candidate will have substantial opportunity to develop his/her own research agenda, preferably directed towards research on consumer credit, fixed income securities, lending and bank risks, real estate, climate risk, and regulatory policies pertaining to these matters.
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Represents the Leukemia Research Program when meeting with Medical Science Liaisons, current and future research collaborators, and prospective donors; assists physician and unit manager in coordinating development plans.
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During the days of your jump deployment, you will perform your duties in an outpatient-based clinic, integrated medical office, or at one of our mobile clinical research sites. Excellent working knowledge of medical and research terminology.
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Additionally support various hull, mechanical and electrical systems (HM&E), and research, development, test and evaluation (RDT&E) programs for the Norfolk Naval Shipyard (NNS) & Naval Surface Warfare Center, Philadelphia Division (NSWCPD.
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Work with PHMC Research & Evaluation Group to develop and submit conference presentations and journal submissions, and participation in selected advisory and strategic planning groups as approved by the Executive Director.
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Research or scholarship responsibilities: Candidates will have an established scholarly program, with an area of concentration in one or more of the following areas: critical care, clinical patient-oriented research, health systems research, medical education, ultrasound, toxicology, emergency medicine services, administrative leadership, global health, resuscitation, laboratory-based basic mechanisms of illness; and other EM-related sub-specialties.
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By building deep relationships with clients and their teams, Executive Partners (EPs): 1) develop a comprehensive understanding of a client’s key priorities, company environment, and personal aspirations; 2) provide candid, actionable feedback on strategies/initiatives; 3) help each client identify and make decisions critical to success; and 4) bring the best of the Forrester ecosystem (spanning research, consulting, and events) to clients in a timely and tailored fashion.
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Posting Summary Rutgers University-Camden is in search of a Director of Grants and Contracts who will report directly to the Vice Chancellor for Research. Under limited supervision, the Director of Grants and Contracts will manage post-award activities related to all campus research funds.
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WHAT YOU NEED TO KNOW (Job Overview): As part of a defined training plan, this position is reporting the Laboratory Director and includes participation in multi-disciplinary research in collaboration with clinical teams, lead quality improvement initiatives, contribute to process improvements, develop, and validate new procedures, and train lab staff, medical students, residents, and fellows.
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The Sidney Kimmel Comprehensive Cancer Center (SKCCC) and the Department of Medical Oncology at TJU in Philadelphia, Pennsylvania is excited to announce a new faculty position who will serve as the Associate Director (AD) of Population Science in SKCCC and the Chief of the Division of Population Science in the Department of Medical Oncology.
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Reporting to the Director of Research and Evaluation, the Qualitative Research and Reporting Manager will lead the Research team’s qualitative data collection. Familiarity with applied research designs especially formative/process-oriented program evaluationExperience in managing proprietary and sensitive dataCommunity organizing or political campaign experienceIf you feel ready to complete the duties of the position, despite not possessing every listed qualification, CEO still encourages you to apply.
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They will be exclusively responsible for generating non-clinical pharmacology data packages to support global health authority (HA) filings. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity/expression, national origin, disability, medical condition, age, marital status, status as a protected veteran, or any other legally protected characteristic.
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research job Title: global medical director Company: Pfizer in Philadelphia, PA
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