- Cedars-Sinai (Beverly Hills, CA)
- …+ **Regulatory Compliance:** Utilize knowledge of regulating agencies (FDA, USP, TJC, DEA, IRB , Board of Pharmacy, etc.), best practice standards, and ... seeking a highly motivated and experienced Supply Chain Pharmacy Coordinator to join our team in Los Angeles, CA....practice standards. + **Decision Support and Best Practices:** Create, review , and coordinate decision support tools and content to… more
- Cedars-Sinai (Beverly Hills, CA)
- …If hired you must reside in the commutable area.** The Research Nurse Coordinator I is responsible for all activities associated with clinical study coordination, ... required and ensures protocol is followed. + May prepare IRB submissions. + May process, ship, track or otherwise...**Req ID** : 7419 **Working Title** : Research Nurse Coordinator I, Oncology (Hybrid) **Department** : Cancer - SOCCI… more
- Actalent (Merced, CA)
- …Research Coordinator Key Responsibilities: + Manage regulatory submissions, including IRB documentation + Serve as the primary point of contact for sponsors ... (excluding budget and contracting) + Conduct informed consent discussions with patients + Coordinate scheduling for standard-of-care procedures + Ensure accountability and compliance for Investigational Products (IP) + Collaborate with nursing staff for blood… more
- Providence (Fullerton, CA)
- …Under the supervision of the Medical Office Administrator, the Clinical Research Coordinator oversees the day to day functions of multiple clinical research studies. ... responsible for interfacing with the Principal Investigator, Patient, Sponsor, and the IRB . This position is directly responsible to ensure that all documentation is… more
- Cedars-Sinai (Los Angeles, CA)
- …contact for long-term follow-up patients only. + Assists with regulatory submissions to the Institutional Review Board ( IRB ) including submission of ... I member will work directly with a Clinical Research Coordinator , Research Program Administrator, or Research Nurse to coordinate...billing. This role will follow all federal, local, FDA, IRB , and HIPAA guidelines and regulations pertaining to the… more
- The County of Los Angeles (Los Angeles, CA)
- …evaluation and genetic research evaluation, as well as grant writing and interaction with the Institutional Review Board ( IRB ). + Provides education to ... in connecting vulnerable populations, including those released from correctional and institutional settings to supportive housing. THE MISSION: To advance the health… more
- Stanford University (Stanford, CA)
- …for completion and accuracy with source documents. Prepare regulatory submissions, and ensure institutional Review Board renewals are completed. + Assemble ... School of Medicine is seeking a 6 month Fixed Term Clinical Research Coordinator Associate to perform duties related to the coordination of clinical studies. The… more
- Rady Children's Hospital San Diego (San Diego, CA)
- …Nurse, under the direction of the Principal Investigator and Clinical Research Coordinator , is responsible for the implementation and for the direct execution and ... research protocol procedures and maintaining compliance with all applicable institutional , state and federal regulations. Other duties include performing regulatory… more