Senior Clinical Research Associate - Remote Position Puma Biotechnology IncSenior Clinical Research Associate - Remote PositionLos Angeles, CARemote$140,000–$165,000 / yearConducts all activities involved in on-site visits consistent with the applicable Clinical Monitoring Plan (CMP), SOPs, and ICH GCP for site qualification, site initiation, interim monitoring, site close-out, and other site visits (eg, booster visits). The physical demands of the home office are normally associated with extended amounts of time sitting and using office equipment (including a computer, keyboard, and mouse), standing, walking, sitting, speaking, and hearing.
Supervisor Clinical Research Coordinator (Orthopedics) Rady Children's HealthSupervisor Clinical Research Coordinator (Orthopedics)Orange, CAStudy management includes but is not limited to assessing feasibility of clinical research protocols, preparing materials needed for regulatory review and submission to the Institutional Review Board (IRB), identifying potential study participants, coordinating and collecting research data/specimens, completing study records in an accurate and timely manner, participating in quality assurance audits, managing study materials and supplies, communicating across multiple teams, and archiving records in accordance with appropriate policies and procedures. Physical Activity Requirements: Bending, Carry Objects, Climbing, Keyboard use/repetitive motion, Pinching/fine motor activities, Push/Pull, Reaching forward, Reaching overhead, Sitting, Squat/kneel/crawl (Squad & Knee), Standing, Talk or hear, Taste or smell, Twisting, Walking, Wrist position deviation.
Senior Clinical Research Coordinator - HematologyOncology Santa Monica UCLA Health SystemSenior Clinical Research Coordinator - HematologyOncology Santa MonicaSanta Monica, CA$82,705.68–$133,068.24 / yearThe ideal candidate is an experienced professional or leader who has direct responsibility for the implementation of research activities for one or more studies which may include multicenter clinical trials (both NIH and industry-sponsored), local investigator-initiated clinical trials, and/or programmatic clinical research activities. Interpersonal skills to effectively communicate information in a timely, professional manner and establish and maintain cooperative and effective working relationships with students, staff, faculty, external collaborators and administration and to work as a member of a team.
Clinical Research Advanced Practice Provider West DermatologyClinical Research Advanced Practice ProviderSanta Ana, California$65–$70 / hourThe Clinical Research Nurse Practitioner/Physician Assistant will work closely with the Principal Investigator to support clinical research studies that specifically focus on diabetes and weight management. The Clinical Research Nurse Practitioner/Physician Assistant will work closely with the Principal Investigator to support various clinical research studies at Southern California Clinical Research.
Clinical Research Coordinator ECN Operating LLCClinical Research CoordinatorHuntington Beach, CA$24–$28 / hourThe CRC will coordinate and support all aspects of clinical trials and research studies, including subject recruitment, data collection, regulatory compliance, and specimen handling. Candidates with current Phlebotomy certification or Medical Assistant (MA) certification are strongly preferred , as this role may include specimen collection and basic clinical procedures.
Clinical Research Associate I - Heart Institute - Makkar Team Cedars-Sinai Medical CenterClinical Research Associate I - Heart Institute - Makkar TeamLos Angeles, CAFrom genetic counseling and targeted drug therapies to a growing array of minimally invasive procedures, Cedars-Sinai continues to stand at the forefront of technology, innovation and discovery improving patient outcomes. The Smidt Heart Institute reflects Cedars-Sinai's steadfast dedication to heart disease and research innovation giving patients access to the highest level of care.
Clinical Research Coordinator II (Imaging) Cedars-Sinai Medical CenterClinical Research Coordinator II (Imaging)Los Angeles, CA$60,028.80–$102,044.80 / hourReq ID 17084 Working Title Clinical Research Coordinator II (Imaging) Department IMG Business Sys and Admin Business Entity Cedars-Sinai Medical Center Job Category Academic / Research Job Specialty Research Studies/ Clin Trial Overtime Status EXEMPT Primary Shift Day Shift Duration 8 hour Base Pay $60028.80 The CRC II serves as an important partner to investigators, research teams, sponsors, and regulatory stakeholders, helping ensure clinical trials are conducted accurately, responsibly, and in accordance with applicable requirements.
NewClinical Research Data Associate II - The Angeles Clinic & Research Institute Cedars-Sinai Medical CenterClinical Research Data Associate II - The Angeles Clinic & Research InstituteLos Angeles, CARemote$25.17–$39.01 / hourReq ID 20340 Working Title Clinical Research Data Associate II - The Angeles Clinic & Research Institute Department Angeles Research Inst Business Entity Cedars-Sinai Medical Center Job Category Academic / Research Job Specialty Research Studies/ Clin Trial Overtime Status NONEXEMPT Primary Shift Day Shift Duration 8 hour Base Pay $25.17 - $39.01. 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 II - Medical Group Cedars-Sinai Medical CenterClinical Research Coordinator II - Medical GroupBeverly Hills, CAPrimary Duties and Responsibilities: Establishes and executes 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. This individual will interact with principal investigators, subjects, clinic and research staff, laboratory staff, medical professionals, pharmaceutical staff, and Sponsor representatives to successfully implement research protocols, in compliance with all applicable regulatory requirements.
Senior Clinical Research Associate PSI CRO AGSenior Clinical Research AssociateCAAdvance your career in clinical research and lead challenging full-service projects on the country/regional level while growing with a rapid company, that puts its people first! Experience monitoring complex Oncology trials required; experience with radiopharmaceuticals and/or breast cancer preferred.
Clinical Informatics Analyst Circuit Clinical Solutions IncClinical Informatics AnalystCARemote$25–$35 / hourTopping a long list of innovation and startup awards over the last 5 years - including winning SCOPE's Participant Engagement Award and winning at 43North - Circuit recently won Fast Company's World Changing Ideas Award. Happy: we seek pragmatic optimists - pessimism and ironic dispositions, especially in leadership can kill startups - we seek those who know the world can be improved by those who work hard and smart to change it.
Senior Manager, Clinical Data Management - External Data Management Crinetics Pharmaceuticals IncSenior Manager, Clinical Data Management - External Data ManagementCA$138,000–$172,000 / yearThe role partners closely with external vendors, CROs, and internal cross‑functional stakeholders to set up data transfer agreements (DTAs), validate test files, manage ongoing data transfers, and perform data reconciliation and quality control activities in compliance with ICH‑GCP, 21 CFR Part 11, and internal SOPs. Position Summary: The Senior Manager, Clinical Data Management - External Data Management (CDM‑EDM) is a hands‑on, individual contributor role responsible for executing and owning external (non‑EDC) data management activities for assigned clinical studies.
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.
RN Clinical - 5 W ICU - Full Time 12 Hour Nights (Non-Exempt) (Union) University of Southern CaliforniaRN Clinical - 5 W ICU - Full Time 12 Hour Nights (Non-Exempt) (Union)Los Angeles, CA$45.76–$98.80 / hourOBSERVES 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 - 7 W Surgical ICU - Full Time 12 Hour Nights (Non-Exempt) (Union) University of Southern CaliforniaRN Clinical - 7 W Surgical ICU - Full Time 12 Hour Nights (Non-Exempt) (Union)Los Angeles, CA$45.76–$98.80 / hourOBSERVES 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 N Medical/Surgical Orthopaedics- Part Time 12 Hour Nights (Non-Exempt) (Union) University of Southern CaliforniaRN Clinical - 6 N Medical/Surgical Orthopaedics- Part Time 12 Hour Nights (Non-Exempt) (Union)Los Angeles, California$45.76–$98.80 / hourOBSERVES 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 Nights (Non-Exempt) (Union) University of Southern CaliforniaRN Clinical - 5S Cardiopulmonary ICU - Full Time 12 Hour Nights (Non-Exempt) (Union)Los Angeles, CA$45.76–$98.80 / hourOBSERVES 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) University of Southern CaliforniaRN Clinical - 5S Cardiopulmonary ICU - Full Time 12 Hour Days (Non-Exempt) (Union)Los Angeles, CA$45.76–$98.80 / hourOBSERVES 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.
Licensed Clinical Social Worker - Full Time, Remote Ria Technology Management IncLicensed Clinical Social Worker - Full Time, RemoteCARemoteLicensed Clinical Social Workers must have demonstrated experience delivering evidence based psychotherapy, such as CBT, MI, and trauma informed care and training in addiction. The investment will further the momentum of commercial partnerships that include regional and national health plans, including Anthem Blue Cross Blue Shield, UnitedHealth Group Optum, Beacon Health Options, Highmark Health, and Magellan Health.
FSP Clinical Research Associate 2 - West, Central, and South Regions Fortrea IncFSP Clinical Research Associate 2 - West, Central, and South RegionsCARemote$100,000–$112,000 / yearResponsibilities: Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned -. Ensure the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools by careful source document Monitor data for missing or implausible data.