- Stanford University (Stanford, CA)
- …from potential participants, and collecting questionnaire responses. The coordinator will work under the supervision of the Research Nurse Manager and Principal ... + Assist with the screening, recruiting, and obtaining consent of study participants. Review medical records and/or perform telephone or in-person interviews… more
- Adecco US, Inc. (Ocala, FL)
- …site operations process, which includes recruitment, enrollment, and retention of study participants. Essential Functions: * Conducts clinical studies according ... required to capture all data as specified by a study protocol, and for ensuring subject safety, understanding, and...in basic computer applications * Good interpersonal skills to work in a team environment **Comments** Monday-Friday 9-5 **Pay… more
- Avispa Technology (Palo Alto, CA)
- …Research Coordinator to join the clinical trials office. The successful candidate will work with the team to ensure the safety and well-being of trial participants ... primary contact with research participants, sponsors, and regulatory agencies. Coordinate studies from start-up through close-out. * Determine eligibility of and… more
- System One (Rochester, NY)
- …Responsibilities The clinical Research Coordinator will manage all aspects of a study ensuring adherence to the protocol, GCP, and applicable regulations, including ... participating in the informed consent process, coordinating, and performing all study visit procedures per protocol, managing Investigational Product and study … more
- Cedars-Sinai (Los Angeles, CA)
- …Program Administrator, or Research Nurse to coordinate and/or implement the study . Evaluates and abstracts research data and ensures compliance with protocol ... the IRB. Provides limited patient contact as needed for study and assist with study budget and...professionals and staff. Choose this if you want to work in a fast-paced environment that offers the highest… more
- IQVIA (Durham, NC)
- …cross-functional collaboration to ensure high-quality feasibility outputs that inform study planning and accelerate trial start-up. **Key Responsibilities** + Ensure ... with Global Program Leads (GPLs), Global Trial Leads (GTLs), and study teams to execute feasibility-related objectives. + Perform feasibility activities including:… more
- CommonSpirit Health (Santa Maria, CA)
- …Research Institute. The incumbent has responsibility for the oversight of studies that explore complex medical diseases, which involve specialty and subspecialty ... injections, and other procedures appropriate within the RN scope of + Dispense study medication to research participants under the direction of the PI, and/or… more
- Cedars-Sinai (Los Angeles, CA)
- …Research Program Administrator, or Research Nurse to coordinate and/or implement the study . This role evaluates and abstracts research data and ensures compliance ... the IRB. Provides limited patient contact as needed for study and assist with study budget and...Proficiency in Word, PowerPoint and Excel. + Ability to work independently, set priorities, and handle multiple tasks requiring… more
- Cedars-Sinai (Los Angeles, CA)
- …role?** The Clinical Research Coordinator II works independently providing study coordination including screening of potential patients for protocol eligibility, ... sponsor queries. Responsible for compiling and reporting on each study including information related to protocol activity, accrual data,...professionals and staff. Choose this if you want to work in a fast-paced environment that offers the highest… more
- Teleflex (Minneapolis, MN)
- …Research Associates (CRAs). This individual has knowledge and experience managing study activities from site selection, start-up, to close-out with adherence to ... * Manage a team of in-house and regional CRAs, providing guidance on study conduct, clinical operational and monitoring strategy, as well as professional growth. *… more