Clinical Research Coordinator ATD Technology LLCClinical Research CoordinatorFullerton, CA$45Oncology Clinical Research Coordinator General Summary: Under the supervision of the Medical Office Administrator, the Clinical Research Coordinator oversees the day to day functions of multiple clinical research studies. Minimum 2 years' experience in a clinical research setting where candidate managed patients (consent them, perform vitals/EKG, process labs, dispense medication, complete documentation, enter data).
Clinical Research Coordinator II Velocity Clinical Research, Inc.Clinical Research Coordinator IIHuntington Park, California$30–$36 / hourTemporaryImplement and coordinate assigned clinical trials including start up, vendor management,subject recruitment, source development review, scheduling subjects, protocol training,collection of regulatory documents, conducting visits, ensuring data is entered in a timely manner and all queries are resolved, managing and reporting adverse events, serious adverse events, and deviations, implementing new protocol amendments, providing all close out reports. Overview: Velocity Clinical Research is an owned and integrated research site organization, providing excellence in patient care, high quality data and fully integrated research sites.
NewResearch RN - Clinical Translational Research Center UCLA Health SystemResearch RN - Clinical Translational Research CenterLos Angeles, CA$65.76–$97.76 / hourDemonstrates responsibility for effect on others by respecting others' opinions and ideas, maintaining cooperative and collaborative relationships with co-workers, demonstrating professional control in stressful situations, and readily assisting co-workers while maintaining interdepartmental communication. Working under the guidance of the Unit Director, you will deliver exceptional direct patient care, collaborate with study teams to optimize protocol-specific workflows, and help advance promising innovations from bench to bedside.
NewClinical Vendor Outsourcing Manager CRO Sourcing & Contracts Pyramid Consulting, IncClinical Vendor Outsourcing Manager CRO Sourcing & ContractsLos Angeles, CA$66–$71 / hourKey Requirements and Technology Experience: 5+ years of relevant experience in clinical vendor outsourcing, clinical sourcing, CRO management, clinical contracts, procurement, or related pharmaceutical/biotechnology functions. Key Responsibilities: Lead and support end-to-end sourcing and contracting activities for full-service CROs and clinical vendors supporting clinical development programs.
Senior Clinical Site Budget Specialist ImmunityBio IncSenior Clinical Site Budget SpecialistEl Segundo, CAGuide and support clinical operations departments in the site budgeting process for ImmunityBio trials, as well as investigator initiated trialsincluding the preparation, negotiation and execution of clinical trial budgets, service contracts and agreements. Designated an FDA Breakthrough Therapy, ANKTIVA is the first FDA-approved immunotherapy for non-muscle invasive bladder cancer CIS that activates NK cells, T cells, and memory T cells for a long-duration response.
Clinical Director Neurology UCLA Health SystemClinical Director NeurologyLos Angeles, CA$132,300–$307,100 / yearThis role is responsible for directing practice operations, supporting regional leadership, and partnering with physicians, practice managers, and staff to ensure exceptional patient care, operational excellence, quality outcomes, and an outstanding patient experience. In collaboration with executive and clinical leadership, you will foster a high-performing environment that supports innovation, clinical research, workforce development, and the delivery of world-class healthcare aligned with UCLA Health's mission and strategic objectives.
RN Clinical Services Group Manager Becton Dickinson and CoRN Clinical Services Group ManagerIrvine, CABachelor's Degree in Healthcare Administration, Nursing, or related field, with 8 years of previous related experience with direct healthcare management of large clinical organizations required. USA DC - Washington, DC, USA FL - Miami, USA MO - St Louis, USA MT - Bozeman, USA OH - Cleveland, USA TX - Austin, USA TX - San Antonio, USA UT - Salt Lake City, USA WA - Seattle.
Clinical Research Coordinator (Experienced) - Westside Los Angeles Irvine Center for Clinical Research IncClinical Research Coordinator (Experienced) - Westside Los AngelesLos Angeles, CA$30–$40 / hourFinal compensation offers will be determined based on the candidate''s specific internal level (CRC II - IV), years of relevant clinical trial experience, and applicable clinical certifications (e.g., CCRC, nursing, or phlebotomy license). Our largest area of research is in Alzheimer's Disease prevention and treatment drug trials, and our doctors were the largest contributors in the world to the most recently FDA-approved medication in Alzheimer's Disease.
NewClinical Study Manager Actalent IncClinical Study ManagerLos Angeles, CARemote$50–$70 / hourWe are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing winner for both client and talent service. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.
Clinical Research Coordinator (Experienced) - Long Beach Irvine Center for Clinical Research IncClinical Research Coordinator (Experienced) - Long BeachLong Beach, CA$30–$40 / hourFinal compensation offers will be determined based on the candidate''s specific internal level (CRC II - IV), years of relevant clinical trial experience, and applicable clinical certifications (e.g., CCRC, nursing, or phlebotomy license). Technical Skills: Demonstrated ability to navigate complex clinical trial management systems (CRIO eSource & CTMS) and EDC platforms quickly and accurately.
NewClinical Research Coordinator I / Heart Institute Children's Hospital Los AngelesClinical Research Coordinator I / Heart InstituteLos Angeles, California$65,520–$87,360 / yearFull timePurpose Statement/Position Summary: The Clinical Research Coordinator I assists principal investigators or other study team members with research studies and assists with subject recruitment, data collection, scheduling of study-related activities and follow-up with enrolled subjects. Children’s Hospital Los Angeles is consistently ranked among the top 10 children's hospitals in the nation, delivering world-class care through more than 350 specialized programs and services.
Manager - Clinical Documentation Specialist DeloitteManager - Clinical Documentation SpecialistLos Angeles, CAFull timeExperience using clinical documentation, coding, and quality metrics, including Medicare Severity Diagnosis Related Groups (MS-DRG), All Patient Refined Diagnosis Related Groups (APR-DRG), patient safety indicators, hospital-acquired conditions, present on admission indicators, and risk adjustment measures. Case management or medical coding certification, including Certified Risk Adjustment Coder (CRC), Certified Coding Associate (CCA), Certified Coding Specialist-Physician-based (CCS-P), Certified Coding Specialist (CCS), Certified Professional Coder (CPC), or Certified Case Manager (CCM).
NewAssociate Clinical Research Coordinator - Cancer Research Providence St. Joseph HealthAssociate Clinical Research Coordinator - Cancer ResearchBurbank, CATogether, our 120,000 caregivers (all employees) serve in over 50 hospitals, over 1,000 clinics and a full range of health and social services across Alaska, California, Montana, New Mexico, Oregon, Texas and Washington. The Clinical Research Associate I will function under the supervision of the Clinical Research Supervisor, coordinating and maintaining diverse activities related to clinical trials at the John Wayne Cancer Institute.
NewAssociate Clinical Research Coordinator - Cancer Research Providence Health & ServicesAssociate Clinical Research Coordinator - Cancer ResearchBurbank, CARequsition ID: 456994 Company: Providence Jobs Job Category: Research Job Function: Clinical Support Job Schedule: Full time Job Shift: Day Career Track: Clinical Support Department: 7009 SJCI DFCC CANCER RESEARCH Address: CA Burbank 191 S Buena Vista St Work Location: PMI Disny Cancr Neurovas Cntr-Burbank Workplace Type: On-site Pay Range: $27.92 - $42.73 Our not-for-profit network provides a full spectrum of care with leading-edge diagnostics and treatment, outpatient health centers, physician groups and clinics, numerous outreach programs, and hospice and home care, and even our own Providence High School.
Clinical Nutrition Manager II - Healthcare Sodexo SAClinical Nutrition Manager II - HealthcareLOS ANGELES, CA$89,250–$115,500 / yearLead daily clinical nutrition operations for a large account, system, or multiple contracts, overseeing both non-exempt and entry-level professional staff. You'll oversee daily nutrition services, drive program excellence, and collaborate with multidisciplinary teams to deliver high-quality patient care.
DPS Clinical Research Assistant I - Outcomes Research City of HopeDPS Clinical Research Assistant I - Outcomes ResearchDuarte, CAYour responsibilities will include participant prescreening, recruitment, informed consent support, study visit coordination, data entry and quality review, regulatory file maintenance, audit readiness, and communication with investigators, clinical teams, regulatory staff, sponsors, vendors, and other internal and external collaborators. Join the forefront of groundbreaking research at the Beckman Research Institute of City of Hope, where we''re changing lives and making a real difference in the fight against cancer, diabetes, and other life-threatening illnesses.
Clinical Research Coordinator II Actalent IncClinical Research Coordinator IIGlendale, CA$33–$40 / hourThis role focuses on screening, recruiting, and consenting patients, performing study-related patient visits and procedures, and collaborating closely with data and regulatory teams to ensure accurate documentation and compliance with study protocols. The Clinical Research Coordinator works within a collaborative oncology research team that includes full-time and part-time coordinators, research assistants, data management staff, regulatory staff, and project management support.
Clinical Research Coordinator III Actalent IncClinical Research Coordinator IIILos Angeles, CA$33–$40 / hourThis role focuses on screening, recruiting, and consenting patients, performing study-related patient visits and procedures, and collaborating closely with data and regulatory teams to ensure accurate documentation and compliance with study protocols. The Clinical Research Coordinator works within a collaborative oncology research team that includes full-time and part-time coordinators, research assistants, data management staff, regulatory staff, and project management support.
Project Manager – Clinical Projects - Torrance PolyPeptide USProject Manager – Clinical Projects - TorranceTorrance, CaliforniaYou will help turn customer agreements into clear action plans, guide cross-functional teams through complex deliverables, and play a direct role in supporting programs tied to important pharmaceutical and biotech development. In this role, you will be at the center of clinical project execution, partnering with customers, internal technical teams, Supply Chain, Commercial Operations, Quality, and Site Leadership to keep projects moving forward.
RN Clinical - 4S ICU - Full Time 12 Hour Nights (Non-Exempt) (Union) Keck Medicine of USCRN Clinical - 4S ICU - 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.