- BeOne Medicines (Emeryville, CA)
- …products and/or medical devices * Conduct site visits to determine protocol and regulatory compliance, and prepare required documentation * Develop collaborative ... relationships with investigative sites, and study vendors * Track enrollment status reports to ensure study sites stay on track to meet enrollment goals * Track study-specific status reports to ensure all required information regarding site issues, deviations,… more
- Bristol Myers Squibb (San Diego, CA)
- …integrity bring out the highest potential of each of our colleagues. **On-site Protocol ** BMS has an occupancy structure that determines where an employee is ... required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role: Site-essential roles require… more
- Stryker (Mountain View, CA)
- …coordinates requisite support. + Able to learn and understand basic Internet Protocol (IP) and computer networking requirements as related to Stryker integration ... products. + Able to understand and implement identical installation and integration practices at different locations in order to ensure consistency and serviceability. + Coordinates and books travel arrangements for self, based on job location and in… more
- University of Southern California (Los Angeles, CA)
- …other hospital personnel. The Coordinator is accountable to the Medical Director and Associate Director of CISO and to the Principal Investigators with whom he/she ... not restricted to those listed below. Specific Job Functions I. Research A. Protocol Related 1. On request from supervisor, reviews in-house protocols prior to CIC… more
- Cedars-Sinai (Los Angeles, CA)
- …a moderate degree of proficiency and understanding of research protocol and laboratory procedures, including centrifuging, aliquoting, storing, and shipping ... documents. + Facilitates screening and recruitment of potential patients for protocol eligibility, presenting non-medical trial concepts and details to the patients,… more
- Cedars-Sinai (Los Angeles, CA)
- …II to join our team. The ideal candidate will have a minimum of an Associate Degree or College Diploma and at least 3 years of clinical research coordination or ... planning, projecting resource requirements, and developing systems to ensure protocol compliance and patient safety. + Coordinates administrative functions of… more
- Sharp HealthCare (La Mesa, CA)
- …identifiers.* Verification of order (electronically or written prescription).* Accurately associate the patient to their images and ordered procedure.Review the ... area(s) and appropriate person(s).Consistently participates and document the Universal Protocol (patient verification, side/site marking and time-out) as appropriate.Assists… more
- University of Southern California (Los Angeles, CA)
- …(NCI) sponsored and Cooperative Group studies. Discerns basic data discrepancies/ protocol violations. Assists in obtaining outside documents and study specimen ... procurement and handling. + Attends new protocol start-up orientations. Completes required protocol specific training. + Assists in preparation of audits of… more
- IQVIA (Carlsbad, CA)
- Job Overview: Join our dynamic team as a Clinical Research Associate ! You'll play a pivotal role in monitoring and managing clinical trial sites to ensure compliance ... plans, ensuring project needs are met. Training & Communication: Provide protocol and study training to sites, maintaining regular communication to manage… more
- Stanford University (Stanford, CA)
- …and operation. **POSITION SUMMARY:** In this position, under the direction of the Associate Director and the IRB Chair, you will conduct in-depth protocol ... knowledge and experience. The primary responsibility will be to manage the protocol review process and identify issues, and to independently determine whether the… more