- Takeda Pharmaceuticals (Lexington, MA)
- …to: + Leading and executing Human Factors strategy in compliance with regional regulatory guidance. + Driving and overseeing User Research strategy in compliance ... Protocols and Reports. + Managing Human Factors, Industrial Design, and User Research vendors. + Supporting regulatory Human Factors Information Requests. +… more
- Penn Medicine (Philadelphia, PA)
- …mission of providing the highest level of care to patients, conducting innovative research , and educating future leaders in the field of medicine. Working for this ... leading academic medical center means collaboration with top clinical , technical and business professionals across all disciplines. Today...a large healthcare system. The ultimate goal of the Associate Safety Manager in this position is to improve… more
- University of Michigan (Ann Arbor, MI)
- Clinical Operations Manager **Early Site Maintenance** We are performing updates and maintenance to our applicant experience. As a result, the site will be ... Now **Job Summary** The person in this position will serve as the Clinical Operations Manager for the Regional Alliance for Healthy Schools (RAHS). This position… more
- Lilly (Indianapolis, IN)
- …and testing. This role will collaborate with Data and Analytics colleagues such as the Clinical Data Associate , Clinical Data Manager and other key partners ... data management, database programming or system validation experience in the clinical , pharmaceutical, biotech, CRO or regulatory agency sectors) + Qualified… more
- Grifols Shared Services North America, Inc (Research Triangle Park, NC)
- …with company policies and industrial best practices. + Provides support for research and developmental studies, clinical or commercial manufacturing as needed. ... Protein Discovery Department, and will report to the New Proteins &Technology Associate Director. We are seeking a highly motivated and experienced individual with… more
- AbbVie (North Chicago, IL)
- …to clinical development, quality assurance, technology, data management, and regulatory affairs. + Study Management Associate Organization: The Study ... clinical data is robust, accurate, and usable for regulatory submissions, evidence generation, and advancing clinical ...focuses on improving the efficiency, quality, and speed of clinical trials and research operations. CAP is… more
- Prime Healthcare (Blue Springs, MO)
- …to provide a high quality, comprehensive, and patient centered learning and clinical experience. The Residency Associate Program Director serves as ... Overview As the Internal Medicine Residency Associate Program Director, with oversight and direction from the Program Director, you will lead a dedicated team… more
- Takeda Pharmaceuticals (Boston, MA)
- …coordination with relevant cross-functional teams (including members of medical affairs, clinical development, and outcomes research ; global, regional, or ... the development of scientific communications strategy and deliverables, the ** Associate Director, Scientific Communications Lead, Hematology** proactively defines and… more
- University of Colorado (Colorado Springs, CO)
- **Longmont Certified Nurse Midwife (Open Rank) in the Non-Tenure Clinical Practice Track** **University of Colorado Colorado Springs** **Description** **University ... / Senior Instructor / Assistant Professor (Open Rank) in the Non-Tenure Clinical Practice Track** **Position location: CU Center for Midwifery at Longmont**… more
- University of Colorado (Denver, CO)
- **Longmont Certified Nurse Midwife (Open Rank) in the Non-Tenure Clinical Practice Track** **University of Colorado Denver** Longmont Certified Nurse Midwife (Open ... Rank) in the Non-Tenure Clinical Practice Track-38368 Faculty **Description** **University of Colorado Anschutz Medical Campus** **College of Nursing** **Position… more