- CommonSpirit Health (Santa Maria, CA)
- …+ Minimum 3 years of experience conducting clinical trials required; worked as primary research nurse for at least 5 drug or device trials. + Experience in ... **Job Summary and Responsibilities** **J** **OB** **S** **UMMARY** **/ P** **URPOSE** The Clinical Research Nurse (CRN) works with the CommonSpirit Health … more
- Cedars-Sinai (Los Angeles, CA)
- … Research Nurse to coordinate/implement study . + Evaluates and abstracts clinical research data from source documents. + Ensures compliance with protocol ... **Are you ready to be a part of breakthrough research ?** The Clinical Research Associate...: Cedars-Sinai Medical Center **Job Category** : Academic / Research **Job Specialty** : Research Studies… more
- University of Colorado (Aurora, CO)
- ** Clinical Research Professional** **Description** **University of Colorado Anschutz Medical Campus** **Department: Anna and John J. Sie Center for Down ... + Develop protocol-specific source documents and organize and prepare research materials for research study ...on a year-for-year basis. + One (1) year of clinical research or related experience. **Applicants must… more
- Cedars-Sinai (Los Angeles, CA)
- …to be a part of breakthrough research ?** The Clinical Research Coordinator I works independently providing study coordination, screening of potential ... adverse events, concomitant medication use, protocol compliance, response to study drug . + Maintains accurate source documents...preferred. **Experience and Skills:** + One (1) year of clinical research related experience is required. +… more
- ProMedica Health System (Toledo, OH)
- …the Clinical Research Scientist, you implement investigator-initiated clinical research studies through collaboration with physicians, researchers, ... and research staff. You will develop hypotheses, research methodology, study design, statistical analysis, writing...or database form. + Leads and/ or participates in clinical research teams designed to grow investigator-initiated… more
- Cedars-Sinai (Los Angeles, CA)
- …for. **What will you be doing in this role?** The Clinical Research Coordinator II works independently providing study coordination including screening of ... patient condition, adverse events, concomitant medication use, protocol compliance, response to study drug . + Maintains accurate source documents related to all… more
- Cedars-Sinai (Los Angeles, CA)
- **Job Description** The Clinical Research Coordinator I works independently providing study coordination, screening of potential patients for protocol ... adverse events, concomitant medication use, protocol compliance, response to study drug . Maintains accurate source documents related...or related degree preferred. + One (1) year of clinical research related experience required. **Req ID**… more
- Cedars-Sinai (Los Angeles, CA)
- …learn more, please visit:** Cedars-Sinai Guerin Children's. The Clinical Research Coordinator I works independently providing study coordination, screening ... adverse events, concomitant medication use, protocol compliance, response to study drug . + Maintains accurate source documents...Certification preferred upon hire + One (1) year of clinical research related experience required. + Prior… more
- Cedars-Sinai (Los Angeles, CA)
- **Job Description** The Clinical Research Coordinator I works independently providing study coordination, screening of potential patients for protocol ... patient condition, adverse events, concomitant medication use, protocol compliance, response to study drug . + Maintains accurate source documents related to all… more
- Cedars-Sinai (Los Angeles, CA)
- …expertise in Alzheimer's disease and related dementias. The Clinical Research Coordinator II works independently providing study coordination including ... you have a passion for helping human kind?** The Clinical Research Coordinator II will work with...events, concomitant medication use, protocol compliance, and response to study drug . + Schedules and participates in… more