- Cytel (Sacramento, CA)
- …Medical Communications and Publications, Epidemiology and Regulatory to design post approval studies . + Writes the statistical sections of study protocols, while ... activities in support of Medical Affairs, including contributing to post approval study designs, study protocol and analysis plan development, reviewing and… more
- Gilead Sciences, Inc. (Foster City, CA)
- …in medical monitoring and addressing medical concerns that arise during clinical studies , experience leading study concept and protocol design, and track-record ... You will join an active therapeutic area with phase 3 and 4 PBC studies and global regulatory filings underway or expected, with potential for work across earlier… more
- Kelly Services (Thousand Oaks, CA)
- …with internal teams and external partners (CROs) to ensure efficient execution of studies and successful project outcomes. + ** Study Support:** Assist with the ... **Senior Research Associate** to support bioanalytical and in vivo studies in CNS drug delivery. This role will be...development of study protocols, contribute to study design, and support the preparation of study… more
- Stanford University (Stanford, CA)
- …CRCA will perform duties related to the coordination of clinical studies , consent patients in person, interview patients, monitor follow-up, coordinate collection ... 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)
- …and patients with Alzheimer's disease, Parkinson's disease, and related disorders. These studies collect information on memory and other mental abilities, which we ... primary contact with research participants, sponsors, and regulatory agencies. Coordinate studies from startup through close-out. + Determine eligibility of and… more
- GRAIL (Menlo Park, CA)
- …we are using the power of next-generation sequencing (NGS), population-scale clinical studies , and state-of-the-art computer science and data science to overcome one ... management activities for one or multiple diagnostic product development studies in support of GRAIL's robust clinical development pipeline. **Responsibilities:**… more
- Stanford University (Stanford, CA)
- …clinical staff, researchers, outside vendors, and other staff to administer treatment and study protocols. May coordinate multi-site studies . + Conduct study ... protocol defined medications, treatments and vaccines in compliance with study protocols. As an integral team member of the...integral team member of the CTRU, you will support study conduct while ensuring the safety of each research… more
- Stanford University (Stanford, CA)
- …studies . **Duties include*:** + Oversee subject recruitment and study enrollment goals. Determine effective strategies for promoting/recruiting research ... Independently manage significant and key aspects of a large study or all aspects of one or more small...requests and questions. + Collaborate with principal investigators and study sponsors, monitor and report serious adverse events, and… more
- Translational Research in Oncology (Los Angeles, CA)
- …perform query resolution in a timely manner to ensure clean data availability for studies analyses + Input and maintain study information in tracking systems: ... but will require travel. Responsibilities: + Monitor activities at assigned clinical study sites to assure adherence to ICH GCPs, local regulatory requirements, TRIO… more
- BeOne Medicines (Emeryville, CA)
- …together with the regional strategic feasibility teams. Close partnership with global program & study management team for design and delivery of the studies , for ... regions to advise quality decision making at TA, indication, program and study levels + Partners with internal stakeholders including global clinical program… more