- Stanford University (Stanford, CA)
- …high degree of professionalism, initiative and flexibility. Responsibilities include assisting in clinical trials such as data entry, study kit preparation, and ... and processing. + Collect and manage patient and laboratory data for clinical research projects. Manage research...report forms. + Ensure compliance with research protocols, and review and audit case report forms for completion and… more
- Stanford University (Stanford, CA)
- …of study specimens and processing. + Collect and manage patient and laboratory data for clinical research projects. Manage research project databases, develop ... Cancer Clinical Research Coordinator Associate - Early Drug Development...and well-being of trial participants and to document related data per protocols and SCI-CTO SOPS and guidelines. Stanford… 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 manage systems to organize, collect, report, and monitor data collection. Extract, analyze, and interpret data ....bodies, which include HIPAA and FDA regulations, + Institutional Review Board requirements, and Good Clinical Practices.… more
- J&J Family of Companies (Irvine, CA)
- …including protocol development, cross functional collaboration for approvals, ensuring compliance for data collection, and data review . + Represents the ... for humanity. Learn more at https://www.jnj.com **Job Function:** Discovery & Pre- Clinical / Clinical Development **Job Sub** **Function:** Clinical … 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 (CA)
- …Institutional Review Board. + Maintains research practices using Good Clinical Practice (GCP) guidelines. + Maintains strict patient confidentiality according to ... **Job Description** **Come join our team!** The Clinical Research Coordinator II works independently providing study coordination including screening of potential… more
- Cedars-Sinai (Los Angeles, CA)
- …technologies. In addition, the position will also offer experience with other technicians, with clinical trials, collecting clinical data , and play a crucial ... patients for research visits and research procedures. + Enters clinical research data into Electronic Data...only. + Assists with regulatory submissions to the Institutional Review Board (IRB) including submission of Adverse Events, Serious… more
- Cedars-Sinai (Beverly Hills, CA)
- …Responsible for directing and managing a specified program within the clinical research operations unit, department, or division. Provides leadership, guidance and ... direction for the day-to-day clinical research operations and activities, including authority to make...May manage the research study intake process, including feasibility, review and endorsement and PRMC submission, as well as… more
- Gilead Sciences, Inc. (Santa Monica, CA)
- …help create more tomorrows. **Job Description** + The **Senior Manager, Planisware Clinical Trial Planning, Resource Management, and Reporting** is a member of the ... and Business Operations team within Development.The role is accountable for ** clinical trial planning activities using Planisware** 1.) accuracy of the critical… more
- Cedars-Sinai (Los Angeles, CA)
- …strive for. **Join our team and contribute to groundbreaking research.** The Clinical Research Specialist provides clinical research expertise by participating ... and coordinate department-wide initiatives such as research quality management or clinical trial recruitment efforts. Ensures compliance with all federal and local… more