- Stanford University (Stanford, CA)
- …+ Assist with the screening, recruiting, and obtaining consent of study participants. Review medical records and/or perform telephone or in-person interviews ... to gather data, as needed. + Administer standard study questionnaires and tests, score test measurements and questionnaires,...accuracy. + Extract data from source documents for research studies as directed. Collect data and complete case report… more
- Parexel (Sacramento, CA)
- …scientific questions, provide daily medical support to Parexel staff or site (investigator/ study coordinator), as needed + Review and sign off adverse events report ... for accuracy and clinical importance, relationship to the study drug as well as for severity and seriousness; provide sponsors with periodic experience reports… more
- Stanford University (Stanford, CA)
- …people from the community and from Stanford University to participate in studies ; run subjects in experimental protocols, organize and maintain data files, and ... assist with study related paperwork. Previous experience working with human subjects...Assist with the screening, recruiting, and obtaining consent of study participants. Perform telephone or in-person interviews to gather… more
- University of Southern California (Los Angeles, CA)
- …cases performed across 7 MRIs (~30% under general anesthesia) + 95,000 General Radiology studies + 12,000 CT scans + 1,000 Nuclear Medicine scans (plus 1500 PETS) + ... Group (CIBORG) specializes in quantitative and computational methods to study brain anatomy and function through magnetic resonance imaging...resonance imaging (MRI). + HEALthy Brain and Child Development Study (HBCD), a 25-site study on brain… more
- Stanford University (Stanford, CA)
- …Positron Emission Tomography and MRI (PET/MRI), and Computed Tomography (CT) to study musculoskeletal conditions. The position is a temporary, 1-year contract with ... + Assist with the screening, recruiting, and obtaining consent of study participants. Review medical records and/or perform telephone or in-person interviews… more
- Sumitomo Pharma (Sacramento, CA)
- …is responsible for the leadership, development, and management of clinical studies while building and maintaining relationships with investigators and key opinion ... and emerging issues. + Oversee project-related education of investigators, study site personnel, and study staff. + Responsible for leading clinical study … more
- Cedars-Sinai (Los Angeles, CA)
- …Research Nurse, or Principal Investigator to coordinate and/or implement the study . The CRAI evaluates and abstracts research data and ensures compliance ... as well as providing limited contact with research participants as needed for study and assists with study /long term follow-up research participants only.… more
- Sumitomo Pharma (Sacramento, CA)
- …Trial Master File (TMF) Specialist will be responsible for ensuring that SMPA studies have comprehensive and quality Trial Master Files (TMFs) ready for audits and ... and system work instructions. Provide support and guidance to study team members during the full lifecycle of the... team members during the full lifecycle of the study , including planning, set-up, maintenance, QC and closure of… more
- Merck (South San Francisco, CA)
- …Drive the publication of biomarker and translational research for respective studies . + Analysis, interpretation & impact: collaborate with forementioned line ... analysis plans, participate in data analysis and interpretation. Effectively communicate the study plan, update and output across different function areas to for… more
- Amgen (South San Francisco, CA)
- …strategies for translational approaches to support clinical dosage selections and clinical study designs. Your impact will extend across therapeutic areas such as ... M-PBPK modeling, M-PBPK-PD modeling, and QSP modeling to inform clinical study designs, optimal dosage selection in target patient populations, characterization of… more