- Alameda Health System (Oakland, CA)
- …adhering to federal regulations and ICH Guidelines, with an emphasis on good clinical practice and clinical Safety Data Management. Administers informed ... consent, enrollment of participants into clinical trials. INSTITUTIONAL REVIEW BOARD (IRB):Acts as departmental representative at Institutional Review … more
- IQVIA (Anaheim, CA)
- …quality deliverables on time and within budget, to customer satisfaction. Provide comprehensive data management expertise to Clinical Data Management (CDM) ... task (eg, Subject Matter Expert (SME). Comply with Good Clinical Practices (GCPs), applicable regulatory guidelines, SOPs, policies, and,...are assigned to meet project deliverables. + Create and/or review and sign-off on all data management… more
- Parexel (San Francisco, CA)
- …/Computer Science, OR equivalent industry experience. + 7+ years experience in pharmaceutical/biotech clinical data management / Biometrics ( clinical trial ... + Experience in leading DM study teams, overseeing trial data activities, and collecting clinical trial and/or...compliant data . + Use surveillance tools to review data at an aggregate level, identifying… more
- Stanford University (Stanford, CA)
- …strategies for promoting/recruiting research participants and retaining participants in long-term clinical trials. + Oversee data management for research ... and regulatory or governing bodies, which include HIPAA and FDA regulations, Institutional Review Board requirements, and Good Clinical Practices. + Knowledge of… more
- Stanford University (Stanford, CA)
- …strategies for promoting/recruiting research participants and retaining participants in long-term clinical trials. + Oversee data management for research ... and regulatory or governing bodies, which include HIPAA and FDA regulations, Institutional Review Board requirements, and Good Clinical Practices. + Knowledge of… more
- Stanford University (Stanford, CA)
- …strategies for promoting/recruiting research participants and retaining participants in long-term clinical trials. + Oversee data management for research ... and regulatory or governing bodies, which include HIPAA and FDA regulations, Institutional Review Board requirements, and Good Clinical Practices. + Knowledge of… more
- Abbott (Sylmar, CA)
- …Customer in product development cycle, and drives the translation into new projects through clinical review and evaluation. + Lead the work with field and ... them to on-time and high quality completion. + Drives, Develops and directs pre- clinical evaluation protocols, data analysis, and reports + Reports significant… more
- Stanford University (Stanford, CA)
- …strategies for promoting/recruiting research participants and retaining participants in long-term clinical trials. + Oversee data management for research ... and regulatory or governing bodies, which include HIPAA and FDA regulations, Institutional Review Board requirements, and Good Clinical Practices. + Knowledge of… more
- Cedars-Sinai (Los Angeles, CA)
- …Institutional Review Board. + Maintains research practices using Good Clinical Practice (GCP) guidelines. + Maintains strict patient confidentiality according to ... **Requirements:** + Bachelor's Degree required. + 5 years of experience in clinical research, regulatory, or data coordination required. + Experience with… more
- Gilead Sciences, Inc. (Foster City, CA)
- …our strategic vision for advanced analytics, with the goal of optimizing clinical trials, enhancing data -driven decision-making, and providing support for ... advisor to help them understand the potential of advanced analytics and apply data -driven approaches to optimize clinical trial operations. + **Stay Ahead:**… more