- Cedars-Sinai (Los Angeles, CA)
- …travel. The Clinical Research Associate I works directly with a Clinical Research Coordinator , Research Program Administrator, or Research Nurse to ... and patient care. **Primary Duties and Responsibilities** + Works with a Clinical Research Coordinator , Research Program Administrator or Research Nurse to… more
- Cedars-Sinai (Los Angeles, CA)
- …The Clinical Research Associate II works directly with a Clinical Research Coordinator , Research Program Administrator, or Research Nurse, or ... and patient care. **Primary Duties and Responsibilities** *Works with a Clinical Research Coordinator , Research Program Administrator, Research Nurse, or… more
- Cedars-Sinai (Los Angeles, CA)
- …The Clinical Research Associate I works directly with a Clinical Research Coordinator , Research Program Administrator, or Research Nurse to ... and patient care. **Primary Duties and Responsibilities** *Works with a Clinical Research Coordinator , Research Program Administrator or Research Nurse to… more
- Cedars-Sinai (Los Angeles, CA)
- … Clinical Research Associate I/CPT works under the direction of a Clinical Research Coordinator , Research Program Administrator, Research Nurse, or other ... **Primary Duties and Responsibilities** + Works under the direction of a Clinical Research Coordinator , Research Program Administrator, Research Nurse, or other… more
- J&J Family of Companies (Irvine, CA)
- …claims and messaging; . Manages and/or mentors resources assigned to designated clinical studies to provide quality deliverables while maintaining optimal ... coordination of all new safety initiatives; o Development of clinical study safety management plan (SMP) and...sites, regulatory, data management) on safety activities related to clinical studies and guarantee adherence to the… more
- J&J Family of Companies (Irvine, CA)
- …+ Strategic planning and coordination of all new safety initiatives; + Development of clinical study safety management plan (SMP) and study -specific safety ... clinical research; + Cooperation with the necessary stakeholders ( clinical study team, medical, clinical ...sites, regulatory, data management) on safety activities related to clinical studies and guarantee adherence to the… more
- University of Southern California (San Diego, CA)
- …Certifications: Certified Clinical Research Associate (CCRA) and/or Certified Clinical Research Coordinator (CCRC). Preferred Experience: 4 years Preferred ... project manager for one or more of the various studies conducted at ATRI under the supervision of the...and verbal communication skills to express complex ideas to study staff at research and clinical institutions.… more
- Cedars-Sinai (Los Angeles, CA)
- …Duties and Responsibilities:** + Obtains patient consent, if authorized, to participate in clinical study . + Engages with OR staff to ensure informed, accurate, ... The CRA I member will work directly with a Clinical Research Coordinator , Research Program Administrator, or...and processing of specimens in the context of the clinical study . + Works with, handle, and… more
- University of Southern California (San Diego, CA)
- …Certifications: Certified Clinical Research Associate (CCRA) and/or Certified Clinical Research Coordinator (CCRC). Preferred Experience: 5 years Preferred ... management. Excellent written and verbal communication skills to express complex ideas to study staff at research and clinical institutions. Ability to handle… more
- IQVIA (Carlsbad, CA)
- …or at least three months of on-site monitoring experience. 2 years of clinical research coordinator experience strongly preferred. + Alternatively, you should ... regular lines of communication plus administering protocol and related study training to assigned sites + Evaluating the quality...will also have a good basic knowledge of applicable clinical research regulatory requirements. You should have: + A… more