- 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
- University of Miami (Miami, FL)
- …diseases circulating in the community. Collect and compile surveillance data. Abstract clinical data from various internal documentation sources and enters data into ... internal and external databases. Integrate regulatory requirements. Use standardized definitions for the identification and classification of events (ie,… more
- Dana-Farber Cancer Institute (Boston, MA)
- …technology and data analytics to enhance patient care, provider experience, clinical research , and operational efficiency. The selected individual is ... informatics to improve patient outcomes, streamline workflows, and advance cancer research . ** Clinical Informatics** : + Oversee the implementation and… more
- University of Utah (Salt Lake City, UT)
- …Understanding of HIPAA / HITRUST compliance and healthcare cybersecurity + Knowledge of clinical research workflows and IRB / regulatory requirements + ... Understanding of security best practices and threat detection + Familiarity with clinical research systems (REDCap, OpenSpecimen) and biorepository workflows +… more
- Lilly (Indianapolis, IN)
- …teams to identify, develop and implement strategies to fully characterize, minimize and monitor the impact of immunogenicity on clinical outcome (benefit and ... expertise (including investigator start-up meetings, IRB, research organizations, research cooperative groups, regional business unit staff, regulatory … more
- Tufts Medicine (Boston, MA)
- …as well as specialized research training in the Institute for Clinical Research and Health Policy. The Cardiovascular Disease Fellowship Programs expose ... Research & Innovation (CVCRI), dedicated to fostering new approaches to clinical research , innovation, education and patient outcomes through an integrated… more