Clinical Research Coordinator II, Neuroscience (Grant Funded) Rady Children's HealthClinical Research Coordinator II, Neuroscience (Grant Funded)Orange, CAPhysical 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. Lifting (Floor to waist level) - Constant 67 or more%, Lifting (Floor to waist level) - Frequent 36-66%, Lifting (Floor to waist level) - Occasional 0-35%, Lifting (Waist level and above) - Constant 67 or more%, Lifting (Waist level and above) - Frequent 36-66%, Lifting (Waist level and above) - Occasional 0-35%.
Clinical Research Coordinator The Los Angeles Cancer NetworkClinical Research CoordinatorFountain Valley, CaliforniaThe Clinical Research Coordinator 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. In collaboration with the physician and other medical personnel, documents thoroughly on Case Report Forms (CRFs) the following: changes in patient condition, adverse events, concomitant medication use, protocol compliance, response to study drug.
Director, Clinical Site Velocity Clinical Research IncDirector, Clinical SiteVan Nuys, CA$140,000–$160,000 / yearThe Clinical Site Director oversees and manages all aspects of the clinical trial process including study feasibility, clinic staffing, patient recruitment, study conduct and regulatory compliance. We are committed to making clinical trials succeed by generating high quality data from as many patients as possible, as quickly as possible while providing exemplary patient care at every step.
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.
Clinical Affairs Manager Innova Medical Group IncClinical Affairs ManagerPasadena, CAInnova Medical Group, Inc. delivers better global health outcomes with its deep expertise in testing and unique offerings in diagnostic medical devices and services that help tackle some of the world's most challenging healthcare problems. In response to the global pandemic, Innova developed an end-to-end ecosystem of rapid diagnostic and screening tests, along with digital reporting and tracing applications to help organizations manage the COVID-19 crisis.
Dietary Aide - Clinical Research CenExelDietary Aide - Clinical ResearchLos Alamitos, CaliforniaSpecialty 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 Trials Regulatory Specialist 2 (Remote Opportunity) Stanford UniversityClinical Trials Regulatory Specialist 2 (Remote Opportunity)CARemoteYou will engage with company sponsors, clinical research organizations, Stanford investigators and their study teams, the Stanford Institutional Review Board (IRB), other external IRBs, the FDA, and various regulatory authorities, as well as any other entities that contribute to clinical research at our institution. CRH is seeking a mission-driven Clinical Trials Regulatory Specialist 2. In this role, you will collaborate with a high-performing team of clinical operations staff and medical experts.
NewClinical Research Nurse - Intermittent Schedule ParexelClinical Research Nurse - Intermittent ScheduleGlendale, CaliforniaPerform or arrange for phlebotomy, urine collection, sample preparation, storage and shipment of samples, drug dispensing, and follows GCP quality study documentation. In addition to base salary, some roles may be eligible for participation in Parexel’s annual performance-based bonus plan, annual salary review and additional total rewards incentives.
Clinical Research Specialist II, Data Collection and Chart Abstraction (Durational with Benefits) Kaiser PermanenteClinical Research Specialist II, Data Collection and Chart Abstraction (Durational with Benefits)Pasadena, CAContributes to the execution of research studies by: conducting research surveys, focus groups, qualitative interviews, or other data gathering activities for straightforward projects or complex projects with guidance; assisting and/or leading the training of others on project support activities (e.g., data collection, administering informed consent, conducting procedures), under the guidance and supervision of more experienced team members; coding open-ended/qualitative responses and preparing data for analysis; reviewing data for accuracy and checking for inconsistencies in data; independently performing tasks related to the recruitment, enrollment, consenting, and follow-up with participants; and answering participant questions regarding basic studies, while serving as a resource to more junior personnel, and escalating issues as needed. Contributes to the execution of research by conducting data gathering activities, reviewing data for accuracy and checking for inconsistencies in data, and independently performing tasks related to the recruitment, enrollment, consenting, follow-up with participants, and answering participant questions.
Clinical Research Associate II City of HopeClinical Research Associate IIDuarte, CAOur dedicated and compassionate faculty and staff are driven by a common mission: Contribute to innovative approaches in predicting, preventing, and curing diseases, shaping the future of medicine through cutting-edge research. Join the forefront of groundbreaking research at City of Hope where we''re changing lives and making a real difference in the fight against cancer, diabetes, and other life-threatening illnesses.
Senior Manager, Clinical Marketing Edwards Lifesciences CorpSenior Manager, Clinical MarketingIrvine, CA$139,000–$196,000 / yearThe position will be responsible for developing and disseminating the messaging, and working closely with clinician leaders around the body of evidence to support and influence product and business unit development activities, competitive strategies, and educational/promotional materials for multiple high value product launches, programs, and initiatives in the business unit. Create high-impact content for speaker presentations, sales enablement tools, objection handlers, and referral-pathway materials, and lead end-to-end development of key sales trainings that translate clinical evidence into field-ready messaging.
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.
Business Development, Preclinical/Clinical Solutions Senior Manager - West Coast Azenta IncBusiness Development, Preclinical/Clinical Solutions Senior Manager - West CoastCARemote$125,000–$150,000 / yearCross-Functional Collaboration: Work closely with internal teams (project management, marketing, scientific experts & account managers) to ensure alignment of client needs with service offerings, and ensure the successful delivery of projects. As a global leader in R&D genomics services, GENEWIZ, leads the way in providing superior data quality with unparalleled technical support to enable researchers around the world to advance their scientific discoveries faster than ever before.
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.
Director, Clinical Site Velocity Clinical Research, Inc.Director, Clinical SiteVan Nuys, California$140,000–$160,000 / yearFull timeThe Clinical Site Director oversees and manages all aspects of the clinical trial process including study feasibility, clinic staffing, patient recruitment, study conduct and regulatory compliance. 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.
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 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 - 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 - 7 S ICU - Full Time 12 Hour Nights (Non-Exempt) (Union) University of Southern CaliforniaRN Clinical - 7 S 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.
NewRN Clinical - 5 E Tele- Full Time 12 Hour Nights- (Non-Exempt) (Union) University of Southern CaliforniaRN Clinical - 5 E Tele- 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.