- IQVIA (Durham, NC)
- …US based **JOB OVERVIEW** The main purpose of this role is to manage the assigned IRT studies in a way that ensures all patients get the study drug on time and ... study and data integrity are maintained from study go live to close out. An important aspect...bug fixes other than the category of "PMG". + Work with a system design PM, assisting with User… more
- Johns Hopkins University (Baltimore, MD)
- Researchers at Johns Hopkins University conduct clinical trials and clinical studies to discover new ways to prevent and treat diseases and other health problems. We ... will administratively coordinate clinical protocol implementation, typically for a single study . Will ensure the efficient logistical implementation of the study… more
- IQVIA (Parsippany, NJ)
- …Practice (GCP), local regulatory requirements, etc. + Develop and document the study -specific training plan for assigned studies . + Conduct and/or supports ... **Job Summary:** CTL&D Analyst provides support to CTL&D for study -specific training planning within various therapeutic area(s). Service/deliverables include… more
- Emory Healthcare/Emory University (Atlanta, GA)
- …+ Assists in the coordination and implementation of clinical research studies , including participant recruitment, enrollment, and follow-up in accordance with ... study protocols and regulatory requirements. + Reviews medical records...at any time, the coordinator may be required to work during evenings, weekends, or overnight hours to ensure… more
- Actalent (Palo Alto, CA)
- …research participants, sponsors, and regulatory agencies. You will coordinate clinical studies from startup through close-out, ensuring compliance with all protocols ... and regulatory requirements. This role offers the opportunity to work with one of the most renowned academic institutions in the US, providing a unique and rewarding… more
- J&J Family of Companies (Santa Clara, CA)
- …+ Other duties as assigned. **Requirements** . Bachelor's Degree in a scientific field of study or equivalent work experience. . Minimum of 5 years of relevant ... The Sr. Field Clinical Engineer will play a critical role in clinical studies including device training, case support, and ensuring timely data collection for… more
- University of Miami (Boca Raton, FL)
- …monitors subjects' responses. + Conducts initiation visits and registers patients in clinical studies . + Performs study data collection and entry using charts, ... exciting opportunity for a Clinical Research Nurse 1 to work in Boca Raton, FL. The Clinical Research Nurse...1 ensures the integrity and quality of clinical research studies are maintained and conducted in accordance with practice… more
- University of Miami (Miami, FL)
- …and order diagnostic tests. Advises patients about continuing care. The ARNP will work within the oncology service line. CORE JOB FUNCTIONS + Performs and documents ... investigator (PI) through discussion and assessment of diagnoses and ascertain study patient eligibility for a clinical trial, including documentation of criteria… more
- University of Rochester (Rochester, NY)
- …Interferometry, and Ocular Biometry (IOL Master). + Participates in human subject studies . Acquires study certification and completes yearly requirements for ... team members with obtaining their certifications. Ensures equipment is correctly enrolled into studies and updated as required. Works with study centers to… more
- University of Michigan (Ann Arbor, MI)
- …a School-wide position and the appointment could be made in the Educational Studies (ES), Learning, Equity, and Problem-Solving for the Public Good (LEAPS), and/or ... Center for the Study of Higher and Postsecondary Education (CSHPE) programs. Applicants...of Michigan Center for Innovation. **Who We Are** Educational Studies , LEAPS, and CSHPE all have internationally recognized faculty… more