- University of Utah (Salt Lake City, UT)
- …review study documents for IRB approval **Supervision** + Report to PSTO /Adapt Clinical Research Manager + Provide guidance and support to study coordinators ... between study sponsor, investigators, study coordinators as well as regulatory or finance where applicable + Participate in Canvas...and clinical research coordinators. + Supervise PSTO and… more
- University of Washington (Seattle, WA)
- …research universities internationally. The Clinical Trials Office (CTO) supports the clinical research mission of UW Medicine. The CTO is an operational ... new therapies to our patients in compliance with evolving regulatory requirements. **Position Summary** The Clinical Trials...Trials Office (CTO) has an exciting opportunity for a Clinical Research Billing Manager. Reporting to the… more
- Emory Healthcare/Emory University (Atlanta, GA)
- …an academic health system, offering a unique opportunity to build and scale clinical operations, optimize our research and enhance our education prominence. The ... the physician dyad leader to shape the department's business strategy, oversee clinical , research and teaching operations and support administrative functions,… more
- University of Michigan (Ann Arbor, MI)
- Clin Res Project Manager Apply Now **Job Summary** This clinical research coordinator (CRC) position may provide study coordination and/or project management for ... multiple clinical research studies of any complexity. Coordinator...communication of costs, policy changes, fiscal requirements and other regulatory issues 4. Oversee and train other research… more
- Johns Hopkins University (Fort Defiance, AZ)
- …their outcomes are documented appropriately. + Attend weekly IRB meetings to provide regulatory expertise, monitor proceedings, and assist faculty and staff with ... to be trained on GCP. + Familiarity with the regulatory agencies involved in human research and...in related field. + Five years related experience in research administration or clinical trials/medical research… more
- Astellas Pharma (Northbrook, IL)
- …to Statistical Programming + Lead and manage global programming teams supporting clinical trials, regulatory submissions, and post-marketing activities. + Define ... guidance for clinical development (eg ICH, GCP), as well as regulatory requirements which include FDA electronic data submission and CDISC implementation +… more
- Penn Medicine (Philadelphia, PA)
- …leadership and direction in regards to all administrative, financial, regulatory , quality, human resources, patient/employee satisfaction, and clinical ... services, coordination of care across several departments/entities, academic involvement ( research initiatives, resident program), special clinical programs,… more
- Penn Medicine (Philadelphia, PA)
- …leadership and direction in regard to all administrative, financial, regulatory , quality, human resources, patient/employee satisfaction, and clinical ... services, coordination of care across several departments/entities, academic involvement ( research initiatives, resident program), special clinical programs,… more
- Penn Medicine (Plainsboro, NJ)
- …supervision and direction in regards to all administrative, financial, regulatory , quality, human resources, patient/employee satisfaction, and clinical ... services, coordination of care across several departments/entities, academic involvement ( research initiatives, resident program), special clinical programs,… more
- Penn Medicine (Berwyn, PA)
- …supervision and direction in regards to all administrative, financial, regulatory , quality, human resources, patient/employee satisfaction, and clinical ... services, coordination of care across several departments/entities, academic involvement ( research initiatives, resident program), special clinical programs,… more