Clinical Research Coordinator I, Laboratory (Onsite) + CPT1 - The Angeles Clinic & Research Institute Cedars-Sinai Medical CenterClinical Research Coordinator I, Laboratory (Onsite) + CPT1 - The Angeles Clinic & Research InstituteLos Angeles, CAExperience: Minimum of six (6) months of healthcare-related or clinical research experience required Phlebotomy and/or laboratory assistant experience with demonstrated proficiency in applicable job responsibilities One (1) year of experience as a Clinical Research Coordinator, Clinical Research Associate, or Clinical Research Assistant preferred. The Angeles Clinic & Research Institute has established an international reputation for developing new cancer therapies, providing the best in experimental and traditional treatments, and expertly guiding and training the next generation of clinicians.
Clinical Research Specialist I - Guzman Lab - Brain Donation Program / Department of Neurology (Hybrid) Cedars-Sinai Medical CenterClinical Research Specialist I - Guzman Lab - Brain Donation Program / Department of Neurology (Hybrid)Los Angeles, CADr. Guzman's research focuses on spatial transcriptomics, brain banking, and clinicopathologic correlation in disorders including Alzheimer disease, hippocampal sclerosis-associated epilepsy, autoimmune neurologic disease, and related neurodegenerative conditions. The program is a partnership between the Neurology Department and interested patients and families to obtain an autopsy shortly after death to study the brain, spinal cord, and other tissues of individuals with memory disorders.
Clinical Research Data Specialist I - Ouyang Lab Cedars-Sinai Medical CenterClinical Research Data Specialist I - Ouyang LabLos Angeles, CAHis previous work has demonstrated the ability of convolutional neural networks to identify systemic human phenotypes that modify cardiovascular risk previously thought to be not apparent on echocardiographic images and precision phenotyping of cardiac function with higher precision than human interpreters. Our cardiologists, cardiac surgeons and niche care teams treat the full spectrum of heart disease and disorders, while our investigators continue to advance the field with groundbreaking, life-saving research.
Clinical & Research Fellow – Ophthalmology NVISION Eye CentersClinical & Research Fellow – OphthalmologyTorrance, CaliforniaInternAlongside clinical training, the position features a structured educational curriculum including didactic lectures and an interactive journal club to prepare the candidate for medical school or advanced graduate programs. Diagnostic Testing: Measure visual acuity, perform lensometry, test intraocular pressure (tonometry), and run advanced imaging such as Optical Coherence Tomography (OCT) and visual field analyzers.
Clinical Research Coordinator I - Kidney Transplant Cedars-Sinai Medical CenterClinical Research Coordinator I - Kidney TransplantCalifornia, CAThe 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. Principal Responsibilities: Independent study coordination including screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details to the patients, and participating in the informed consent process.
Dietary Aide - Clinical Research Collaborative Neuroscience Research, LLCDietary Aide - Clinical ResearchLos Alamitos, CA$20–$21.50 / hourPart timeSpecialty areas of research across our sites include Psychiatry, Acute Post Op Pain, Asian Bridging, Dermatology, GI, and Neurology. We focus on quality people, teamwork, and highly experienced clinical research managers with a history of success.
Clinical Sales Specialist, Structural Heart - Structural Interventions (Los Angeles, CA) Abbott LaboratoriesClinical Sales Specialist, Structural Heart - Structural Interventions (Los Angeles, CA)Los Angeles, CA$78,000–$156,000 / yearThis particular role is focused on Abbott's Amplatzer Congenital offering which encompasses atrial septal defects (ASD), patent ductus arteriosus (PDA) and ventricular septal defects (VSD), and patent foramen ovale (PFO). In this role, the Clinical Specialist with train interventional cardiologists, catheter lab staff and ancillary personnel on the use of Structural Heart products and provide technical support to physicians during procedures.
Clinical Sales Specialist, Structural Heart - Structural Interventions (Los Angeles, CA) AbbottClinical Sales Specialist, Structural Heart - Structural Interventions (Los Angeles, CA)Los Angeles, California$78,000–$156,000 / yearThis particular role is focused on Abbott’s Amplatzer Congenital offering which encompasses atrial septal defects (ASD), patent ductus arteriosus (PDA) and ventricular septal defects (VSD), and patent foramen ovale (PFO). In this role, the Clinical Specialist with train interventional cardiologists, catheter lab staff and ancillary personnel on the use of Structural Heart products and provide technical support to physicians during procedures.
Clinical Research Data Specialist I (Per Diem) - Heart Institute - Ouyang Lab Cedars-Sinai Medical CenterClinical Research Data Specialist I (Per Diem) - Heart Institute - Ouyang LabLos Angeles, CAHis previous work has demonstrated the ability of convolutional neural networks to identify systemic human phenotypes that modify cardiovascular risk previously thought to be not apparent on echocardiographic images and precision phenotyping of cardiac function with higher precision than human interpreters. Our cardiologists, cardiac surgeons and niche care teams treat the full spectrum of heart disease and disorders, while our investigators continue to advance the field with groundbreaking, life-saving research.
Clinical Research Coordinator I - Medically Associated Science & Technology (MAST) Program Cedars-Sinai Medical CenterClinical Research Coordinator I - Medically Associated Science & Technology (MAST) ProgramLos Angeles, CAThe Clinical Research Coordinator I works independently providing study coordination including screening of patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. In collaboration with the physician and other medical personnel, documents on Case Report Forms (CRFs) the following: changes in patient condition, adverse events, concomitant medication use, protocol compliance, response to study drug.
Clinical Research Coordinator II - The Angeles Clinic & Research Institute Cedars-Sinai Medical CenterClinical Research Coordinator II - The Angeles Clinic & Research InstituteLos Angeles, CAKey Responsibilities: • Establishes and completes logistical aspects of clinical research projects to achieve project objectives, including project planning, projecting resource requirements, and developing systems to ensure protocol compliance and patient safety. The Angeles Clinic & Research Institute has established an international reputation for developing new cancer therapies, providing the best in experimental and traditional treatments, and expertly guiding and training the next generation of clinicians.
Clinical Research Coordinator I - Department of Neurology (Hybrid) Cedars-Sinai Medical CenterClinical Research Coordinator I - Department of Neurology (Hybrid)Los Angeles, CAThe Clinical Research Coordinator I will work independently providing study coordination including screening of research participants for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. • Collaboration with the physician and other medical personnel, documenting thoroughly on Case Report Forms (CRFs) information about changes in research participant condition, adverse events, concomitant medication use, protocol compliance, and response to study drug.
Clinical Research Data Associate II - The Angeles Clinic & Research Institute Cedars-Sinai Medical CenterClinical Research Data Associate II - The Angeles Clinic & Research InstituteLos Angeles, CAExperience: Minimum of two (2) years of relevant experience in clinical research or a related setting Hands-on experience with Electronic Data Capture (EDC) systems, preferably within oncology clinical trials Familiarity with EDC platforms such as REDCap, Oracle Clinical, Veeva Vault, Medidata Rave, and/or OpenClinica Proficiency with data management software and related tools Demonstrated ability to work effectively in a collaborative, team-oriented environment Strong attention to detail with excellent organizational and time-management skills Excellent written and verbal communication skills Proven ability to adhere to regulatory requirements and ethical guidelines. The Angeles Clinic & Research Institute has established an international reputation for developing new cancer therapies, providing the best in experimental and traditional treatments, and expertly guiding and training the next generation of clinicians.
Clinical Program Manager for Quality (BMT/CAR T) - Hybrid Cedars-Sinai Medical CenterClinical Program Manager for Quality (BMT/CAR T) - HybridBeverly Hills, CAJob Summary The Clinical Program Manager (BMT/CAR T Quality in Hematology and Cell Therapy Division) plays a key role in advancing Cedars-Sinais commitment to exceptional patient care by driving operational efficiency, clinical excellence, and value-based outcomes. We offer learning programs, tuition reimbursement and performance-improvement projects so you can achieve certifications and degrees while gaining the knowledge and experience needed to advance your career.
Clinical Research Coordinator III - Cardiology Research - Makkar Lab Cedars-Sinai Medical CenterClinical Research Coordinator III - Cardiology Research - Makkar LabLos Angeles, CAThe Clinical Research Coordinator III 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. The Smidt Heart Institute reflects Cedars-Sinais steadfast dedication to heart disease and research innovation, giving patients access to the highest level of care.
Clinical Research Associate I - Pulmonary Research Program/Lung Institute Cedars-Sinai Medical CenterClinical Research Associate I - Pulmonary Research Program/Lung InstituteBeverly Hills, CAThe Clinical Research Associate I will work under the direction of a Clinical Research Coordinator, Research Program Administrator, Research Nurse, or other supervising staff to assist in tasks supporting the coordination/implementation of noncomplex research studies. The incumbent will support objectives of research studies through noncomplex tasks such as data collection, prescreening of and scheduling of current research participants, assisting in IRB submission activities, budget and billing, and ensuring overall compliance with all federal and local guidelines.
ECM Clinical Care Manager Amity FoundationECM Clinical Care ManagerLos Angeles, California$70,000–$75,000 / yearThe role of the ECM Clinical Case Manager provides integrated clinical and case management services to justice-involved individuals enrolled in Enhanced Care Management (ECM), with a primary focus on in-custody engagement within Orange County jail facilities and post-release community reintegration. This role delivers in-person assessments, pre-release planning, and clinical coordination inside the three Orange County jail facilities, while maintaining continuity of care through post-release case management, clinical touchpoints, and linkage to services in the community.
RN Clinical - 5 W ICU - Full Time 12 Hour Days (Non-Exempt) (Union) Keck Medicine of USCRN Clinical - 5 W ICU - Full Time 12 Hour Days (Non-Exempt) (Union)Los Angeles, CaliforniaOBSERVES REGULATORY AGENCY REQUIREMENTS: National Patient Safety Goals Patient identifiers Unapproved abbreviations Universal Protocol (Procedural Time Out) Hand-Off Medication Reconciliation Clinical Alarms Other Hazardous waste management Biohazard Medication Sharps HIPAA OSHA requirements (i.e. no food or drink in clinical areas) JCAHO – continuous survey readiness Critical Values Write Down Read Back Follow up Telephone order Appropriate Documented Signed, Timed and Dated Stamped Entered into unit log Maintains safe practice in the work environment Correct body mechanics Electrical safety Infection Control Procedures Hand Washing. DOCUMENTATION Documentation is complete and correct on all flow sheets and chart forms: Admission Assessment Pain scale assessment and reassessment before and after intervention Daily flow sheet Restraint flow sheet Diabetes flow sheet Educational flow sheet Kardex Care Plan Risk Assessment & Reassessment upon Fall MAR Equipment & Supplies Intra and Inter Facility Transfer Forms Belonging Tracking Form Ensures orders are transcribed and signed off prior to the end of the shift.
RN Clinical - 5S Cardiopulmonary ICU - Full Time 12 Hour Days (Non-Exempt) (Union) Keck Medicine of USCRN Clinical - 5S Cardiopulmonary ICU - Full Time 12 Hour Days (Non-Exempt) (Union)Los Angeles, CaliforniaOBSERVES REGULATORY AGENCY REQUIREMENTS: National Patient Safety Goals Patient identifiers Unapproved abbreviations Universal Protocol (Procedural Time Out) Hand-Off Medication Reconciliation Clinical Alarms Other Hazardous waste management Biohazard Medication Sharps HIPAA OSHA requirements (i.e. no food or drink in clinical areas) JCAHO – continuous survey readiness Critical Values § Write Down § Read Back § Follow up Telephone order § Appropriate § Documented § Signed, Timed and Dated § Stamped § Entered into unit log Maintains safe practice in the work environment § Correct body mechanics § Electrical safety § Infection Control Procedures § Hand Washing. DOCUMENTATION Documentation is complete and correct on all flow sheets and chart forms: Admission Assessment Pain scale assessment and reassessment before and after intervention Daily flow sheet Restraint flow sheet Diabetes flow sheet Educational flow sheet Kardex Care Plan Risk Assessment & Reassessment upon Fall MAR Equipment & Supplies Intra and Inter Facility Transfer Forms Belonging Tracking Form Ensures orders are transcribed and signed off prior to the end of the shift.
RN Clinical - 6 EW Medical Surgical Stepdown - Full Time 12 Hour Nights (Non-Exempt) (Union) Keck Medicine of USCRN Clinical - 6 EW Medical Surgical Stepdown - Full Time 12 Hour Nights (Non-Exempt) (Union)Los Angeles, CaliforniaOBSERVES REGULATORY AGENCY REQUIREMENTS: National Patient Safety Goals Patient identifiers Unapproved abbreviations Universal Protocol (Procedural Time Out) Hand-Off Medication Reconciliation Clinical Alarms Other Hazardous waste management Biohazard Medication Sharps HIPAA OSHA requirements (i.e. no food or drink in clinical areas) JCAHO – continuous survey readiness Critical Values § Write Down § Read Back § Follow up Telephone order § Appropriate § Documented § Signed, Timed and Dated § Stamped § Entered into unit log Maintains safe practice in the work environment § Correct body mechanics § Electrical safety § Infection Control Procedures § Hand Washing. DOCUMENTATION Documentation is complete and correct on all flow sheets and chart forms: Admission Assessment Pain scale assessment and reassessment before and after intervention Daily flow sheet Restraint flow sheet Diabetes flow sheet Educational flow sheet Kardex Care Plan Risk Assessment & Reassessment upon Fall MAR Equipment & Supplies Intra and Inter Facility Transfer Forms Belonging Tracking Form Ensures orders are transcribed and signed off prior to the end of the shift.