- Stanford University (Stanford, CA)
- …SQL, Python, R, or other appropriate languages. . Compile survey data and clinical research data into usable formats. . Identify relevant publicly available ... Stanford University School of Medicine and the Heart Center Clinical and Translational Research Program (CTRP) are.... Oversee and maintain access to data resources, ensuring compliance with all local and external regulatory … more
- Sumitomo Pharma (Sacramento, CA)
- …management of CROs, consultants and vendors. + Oversees and monitors the management of clinical studies ensuring they are conducted in compliance with the agreed ... of clinical study-related documents such as protocols, protocol amendments, clinical study reports (CSRs), regulatory submissions and other publications as… more
- Dignity Health (Bakersfield, CA)
- …as well as organizational policies and procedures. - Monitor and respond to regulatory changes that impact claims processing and research activities. - Schedule ... **Responsibilities** The Claims Research Specialist will oversee and manage research...- Collaborate with internal departments, including claims processing, UM, compliance , and provider relations, to develop and implement strategies… more
- ThermoFisher Scientific (San Diego, CA)
- … trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, ... career goals while taking science a step beyond through research , development and delivery of life-changing therapies. With ...stability samples for storage and testing. Conducts work in compliance with safety and regulatory requirements. May… more
- Bausch + Lomb (Sacramento, CA)
- …Practices (GCP), clinical trials management (including site monitoring), scientific methods, research design, regulatory compliance , and clinical ... manner. + Oversee the preparation of procedures for the conduct and monitoring of clinical research such as Clinical Monitoring Plans, procedures for… more
- Sumitomo Pharma (Sacramento, CA)
- …of clinical study-related documents such as protocols, protocol amendments, clinical study reports (CSRs), regulatory submissions and other publications as ... and problem solving + Working knowledge of current global regulatory requirements and guidelines for clinical trials....considered confidential. ** Compliance ** : Achieve and maintain Compliance with all applicable regulatory , legal and… more
- Abbott (Alameda, CA)
- …life sciences, medical, bio-medical engineering, or related field. + Minimum 6 years in clinical research or related field. + Education and work experience in ... research compliance , or quality, project management, or...research compliance , or quality,.... + Knowledge of data collection best practices for clinical trials familiarity with regulatory frameworks (eg,… more
- Amgen (Thousand Oaks, CA)
- …certified or equivalent + Ten (10) or more years in biopharmaceutical sponsored clinical research is desirable + Biopharmaceutical experience as a medical ... clinical development colleagues in co-authoring and reviewing clinical sections of regulatory documents + Lead...Compliance Guidelines + Provide medical monitoring oversight for clinical trials as required **Win** **What we expect of… more
- Alameda Health System (Oakland, CA)
- …nursing personnel and non-nursing personnel as indicated for professional development and regulatory compliance . **DUTIES & ESSENTIAL JOB FUNCTIONS** NOTE: The ... Clinical Educator II + Oakland, CA + Highland...employee education files as needed for managers and/or any regulatory agencies. + Assists AHS leadership team during … more
- Cordis (Santa Clara, CA)
- …across the organization. + Able to summarize results of design work and research studies concisely. Participates in the regulatory submission process as a ... design and development expertise in vascular closure devices with relevant clinical application experience, and a good understanding of cardiovascular catheter… more