- Stanford University (Stanford, CA)
- …Research Coordinator Associate to perform duties related to the coordination of clinical studies . The CRCA will coordinate moderately complex aspects of one or more ... clinical studies . The CRCA will work under close direction of...close-out. + Determine eligibility of and gather consent from study participants according to protocol. Assist in developing recruitment… more
- Stanford University (Stanford, CA)
- … studies in all aspects of clinical and translational research studies including regulatory compliance, study implementation, protocol development, data ... three years of demonstrated managerial experience. . Demonstrated disease knowledge / study design experience of studies under purview. **CERTIFICATIONS &… more
- University of Miami (Miami, FL)
- …in the study . + Administers informed consent forms for patients on drug studies . + Maintains pool of study candidates and ensures their availability. + ... FL.The Clinical Research Coordinator provides professional level support for research clinical studies involving human subjects and assists in the design of … more
- Baylor Scott & White Health (Plano, TX)
- …or charging mechanisms are in place for research charges related to research studies . Requires familiarity with research study budgets and provides feedback on ... conducting clinical trials during all phases of trials including pre- study implementation through study closure per federal,...will learn to assist Principal Investigators on more complex studies and seek guidance from more senior roles when… more
- Sanofi Group (Morristown, NJ)
- …to end including: reviewing ISS and ESC applications, liaising with the investigators of study applications, presenting studies to the GMT and SRC, following ... Investigator (PI), and the US Medical Team on Sanofi-sponsored studies , as delegated by the Franchise Medical Head **External...Global Brand Team (GBT) strategies + Liaise with Medical Study Leader to oversee investigator-initiated study (IIS)… more
- Parexel (Glendale, CA)
- …clinical research coordinators, etc. to ensure the enrollment process of study participants is completed safely while following standards and protocols. Starting ... according to protocol specific requirements and CFR/ICH GCP guidelines. Ensure all study laboratory and medical tests are completed and the eligibility requirements… more
- Bristol Myers Squibb (Princeton, NJ)
- …which provides the scientific expertise necessary to design and deliver clinical studies and programs with high quality and urgency. + Individual contributor role ... to represent the CS group in cross-functional initiatives + Ensures consistency across studies within an asset and/or indication + Provides support for clinical … more
- WellSpan Health (York, PA)
- …Monitors and facilitates necessary documentation in the conduct of clinical research studies . Regularly reviews protocol study forms for accuracy and compliance ... evenings **General Summary** Coordinates clinical research activities and compliance to study requirements, and patient and staff considerations relative to specific… more
- Houston Methodist (Houston, TX)
- …This position performs advanced duties including the scoring of sleep studies and preparation of preliminary report for physician interpretation, completing the ... the physician. The Sr Polysomnographic Technologist position conducts sleep studies , including advanced and complex procedures, performing polysomnography, diagnostic… more
- UCLA Fielding School of Public Health (Los Angeles, CA)
- …language models, and machine learning. Examples of the prospective clinical studies include testing the implementation of artificial intelligence algorithms for ... closely related field. Desired skills include experience in biostatistics, study design, trial operations, artificial intelligence, or implementation science.… more