- Sumitomo Pharma (Sacramento, CA)
- …budget management, timelines, resource management, site management, monitoring, study management, vendor management, and project operational support. Drives ... all aspects of study execution in collaboration with cross-functional teams and vendors....monitoring, and successful completion of one or more clinical studies within a program(s), ensuring adherence to timelines, budgets,… more
- Cordis (Irvine, CA)
- …We are seeking a Clinical Trial Associate to join our clinical study team in the peripheral/coronary space to help execute a randomized, multi-center ... various duties and responsibilities as directed by the clinical study leader. This research is the top priority for...CRO or Sponsor setting with strong knowledge of conducting studies under ICH and GCP guidelines **Preferred Qualifications** +… more
- AbbVie (Irvine, CA)
- …oversee the direction, planning, execution, and interpretation of clinical studies and research activities of aesthetic clinical development programs. Participates ... markets, business operations and emerging issues. Oversee project-related training of investigators, study site personnel, and AbbVie study staff. + Oversee… more
- Cordis (Irvine, CA)
- …to this device. In this role, you will be participating in a clinical study team in the coronary space to execute a randomized, multi-center IDE clinical trial. ... various duties and responsibilities as directed by the clinical study leader. This research is the top priority for...CRO or Sponsor setting with strong knowledge of conducting studies under ICH and GCP guidelines + Bachelor's degree,… more
- Cedars-Sinai (Los Angeles, CA)
- …and leading staff. + Provides guidance, instruction and expertise to team members on study requirements and clinical coordination of the studies . + May assist ... III is responsible for all activities associated with clinical study coordination, subject enrollment, data management/integrity, regulatory compliance, project/… more
- Cedars-Sinai (Beverly Hills, CA)
- …is responsible for all activities associated with clinical study coordination, subject recruitment/enrollment, data management/integrity, regulatory compliance, ... and family members. Coordinates the clinical logistics of the study , and works in tandem with the Research and/or...as it pertains to the clinical coordination of the studies . Primary Duties and Responsibilities + Responsible for clinical… more
- 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)
- …more complex projects and assignments. Independently manages significant and key aspects of large studies or all aspects of one or more small research studies . ... primary contact with research participants, sponsors, and regulatory agencies. Coordinate studies from startup through close-out. * Determine eligibility of and… more
- Stanford University (Stanford, CA)
- …Melanoma Clinical Research Group (CRG)Independently manage significant and key aspects of a large study or all aspects of one or more small research studies . ... complex treatment. **Duties include*:** + Oversee subject recruitment and study enrollment goals. Determine effective strategies for promoting/recruiting research… 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