- 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
- Actalent (Palo Alto, CA)
- …research participants, sponsors, and regulatory agencies. You will coordinate clinical studies from startup through close-out, ensuring compliance with all protocols ... in the field of clinical research. Responsibilities + Determine eligibility of study participants and gather consent according to protocol. + Assist in developing… more
- ThermoFisher Scientific (Carlsbad, CA)
- …clinical deliverable (usually clean data from evaluable patients as specified in the study protocol) within the time period specified in the contract with the ... high complexity and may assume regional lead or Clinical Study Manager responsibilities. What You'll Do: + Manage all...Manage all clinical operational and quality aspects of allocated studies , of moderate to high complexity, in compliance with… more
- J&J Family of Companies (Santa Clara, CA)
- …The Sr. Field Clinical Engineer will play a critical role in clinical studies including device training, case support, and ensuring timely data collection for ... to ensure the safe and effective use of medical devices. + Present clinical study training materials based on investigational plans to support the safe and effective… more
- Stanford University (Stanford, CA)
- …Programis seeking an Assistant Clinical Research Coordinator (ACRC) to support the clinical studies . This position is expected to work onsite, engage in all facets ... of research, including study recruitment and enrollment, grant writing, abstract/manuscript writing, designing...accuracy. + Extract data from source documents for research studies as directed. Collect data and complete case report… 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