- J&J Family of Companies (Irvine, CA)
- …with co-workers across the organization. **Key Duties/Responsibilities** + Oversees the study program, ensures compliance with procedures, monitors studies based ... study level execution for pre-market and post-market collaborative studies , including protocol development, cross functional collaboration for approvals, ensuring… more
- US Tech Solutions (Mountain View, CA)
- …research studies . + Manage and support the setup and execution of research studies . + Understand study needs, create research plans, organize study ... and mixed methods research in support of Project. + Support existing number of studies (vision comfort). + The Visual Science Researcher will work closely with other… more
- Stanford University (Stanford, CA)
- …Programis seeking an Assistant Clinical Research Coordinator (ACRC) to support the clinical studies with Dr. Serena Hu. This position is expected to work onsite, ... engage in all facets of research, including study recruitment and enrollment, grant writing, abstract/manuscript writing, designing and implementing their own… more
- Cedars-Sinai (Beverly Hills, CA)
- …university and hospital committees and task forces as assigned. + Clinical Study Coordination: + Independently coordinate studies , including patient screening, ... organizes resources to meet program objectives. + May manage the research study intake process, including feasibility, review and endorsement and PRMC submission, as… more
- Edwards Lifesciences (Irvine, CA)
- …providing scientific expertise throughout the development and implementation of clinical studies and clinical evaluations for a dynamic portfolio of products across ... of clinical science and medical writing deliverables. + Lead clinical study design and clinical protocol development. + Independently author complex documents… more
- Ascendis Pharma (Palo Alto, CA)
- …will be expected to provide timely and strategic programming support to clinical study teams in alignment with project goals. This role combines hands-on programming ... responsibilities with leadership in study execution and tool development. The successful candidate will...specification templates of SDTM and ADaM used across clinical studies . This position requires expertise in CDISC standards (SDTM,… more
- Abbott (Santa Clara, CA)
- … studies . Writes/manages clinical trial protocols, protocol amendments, clinical study reports, clinical trial registrations and results postings, clinical ... project timelines and scientific publications. Interacts with various study support groups cross-functional teams in order to assist...to provide strategic communication to staff as well as study sites as directed by your manager. **What You'll… more
- Genentech (South San Francisco, CA)
- …meaningful improvement to patients. The Clinical Scientist supports the molecule/ study /project team for effective and efficient Clinical Development Plan (CDP) ... execution. This includes contributing to clinical documentation, supporting training of study site personnel, acting as a point-of-contact for questions and… more
- System One (Walnut Creek, CA)
- …Investigator (PI) provides medical leadership and overall oversight for clinical research studies conducted at various US based sites. This PRN role ensures that ... all study activities are performed in compliance with ICH-GCP, FDA,...the main point of contact for sponsors, CROs, and study monitors. Key Responsibilities + Lead and oversee all… more
- Stanford University (Stanford, CA)
- …in Radiation Oncology. Independently manage significant and key aspects of a large study or all aspects of one or more small research studies . ... and flexibility. **Duties include*:** + Oversee subject recruitment and study enrollment goals. Determine effective strategies for promoting/recruiting research… more