- Cedars-Sinai (Beverly Hills, CA)
- **Job Description** **Join our team!** The Clinical Research Coordinator II works independently providing study coordination including screening of potential ... patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. Responsible for accurate and… more
- Actalent (Pasadena, CA)
- …Seeking an experienced Clinical Research Coordinator to manage multiple clinical trials , ensure protocol compliance, and support patient engagement ... throughout the study lifecycle. Key Responsibilities: + Manage 6-8 clinical trials + Conduct patient screening, informed consent, and study visits + Maintain… more
- BeOne Medicines (San Carlos, CA)
- **General Description:** Manage biomarker related operational work for clinical trials and programs. Act as biomarker operation representative to ... the job:** + Independently manage biomarker and bio-sample testing activities for clinical trials , including but not limited to review and finalize lab vendors… more
- Cedars-Sinai (Los Angeles, CA)
- **Job Description** The Clinical Research Coordinator I works independently providing study coordination, screening of potential patients for protocol eligibility, ... presenting non-medical trial concepts and details, and participating in the informed...Institutional Review Board. + Maintains research practices using Good Clinical Practice (GCP) guidelines. + Maintains strict patient confidentiality… more
- Cedars-Sinai (Los Angeles, CA)
- …where they live and work, ensuring meaningful community engagement. The Clinical Research Coordinator I works independently providing study coordination, screening ... of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. Responsible for… more
- BeOne Medicines (Emeryville, CA)
- …and safety section for clinical data management plan for capture during clinical trials , supports the review and update of data management plan based ... to BeiGene employees on product safety issues and profiles ** Trial Safety** **Support:** + Accountable for safety data, reviews...of safety data required for capture in CRFs during clinical trials , reviews and provides product program… more
- Actalent (Irvine, CA)
- … Study Assistant will be responsible for: - Administrative support of the clinical trials department - Coordination and building of study documentation binders ... Sites - Ensures completeness and accuracy of internal documents related to clinical trials - Compiling required regulatory and financial documentations to… more
- Cedars-Sinai (Los Angeles, CA)
- …and Safety Letters in accordance with local and federal guidelines. Assists with clinical trial budgets and patient research billing as needed Schedules patients ... known nationally for excellence in research!** **Job Summary:** The Clinical Research Associate I works directly with a ...Academic / Research **Job Specialty** : Research Studies/ Clin Trial **Overtime Status** : NONEXEMPT **Primary Shift** : Day… more
- Cedars-Sinai (Los Angeles, CA)
- …and Safety Letters in accordance with local and federal guidelines. + Assists with clinical trial budgets. + Assists with patient research billing. + Schedules ... **Job Description** The Clinical Research Associate I works directly with a...Academic / Research **Job Specialty** : Research Studies/ Clin Trial **Overtime Status** : NONEXEMPT **Primary Shift** : Day… more
- Cedars-Sinai (Los Angeles, CA)
- …and Safety Letters in accordance with local and federal guidelines. + Assists with clinical trial budgets. + Assists with patient research billing. + Schedules ... enduring, precision treatment to patients around the world. The Clinical Research Associate I works directly with a ...Academic / Research **Job Specialty** : Research Studies/ Clin Trial **Overtime Status** : NONEXEMPT **Primary Shift** : Day… more