NewPediatrics - Endocrinology Clinical Faculty Cedars-Sinai Health SystemPediatrics - Endocrinology Clinical FacultyLos Angeles, CA$218,000–$322,400 / yearThe total pay range shown takes into account the wide range of factors that are considered in making compensation decisions including knowledge/skills; relevant experience and training; education/certifications/licensure; and other business and organizational factors. For mid-career candidates with demonstrated leadership experience or administrative potential, leadership opportunities may be available in areas including clinical program development, quality, patient safety, operations, and strategic growth.
NewClinical Value Nurse Practitioner (NP) - Department of Medicine - 8 Hour Day Shift Cedars-Sinai Health SystemClinical Value Nurse Practitioner (NP) - Department of Medicine - 8 Hour Day ShiftLos Angeles, CAExperience: Two (2) plus years of clinical and healthcare operations experience with demonstrated success leading value-based care, care management, population health, quality improvement, or clinical efficiency initiatives. Strong experience collaborating with physicians and multidisciplinary teams to reduce length of stay, improve care transitions, reduce readmissions, and achieve quality and cost-performance goals.
NewPediatric Hospitalist Clinical Faculty Cedars-Sinai Health SystemPediatric Hospitalist Clinical FacultyLos Angeles, CA$227,000–$334,800 / yearThe total pay range shown takes into account the wide range of factors that are considered in making compensation decisions including knowledge/skills; relevant experience and training; education/certifications/licensure; and other business and organizational factors. For mid-career candidates with demonstrated leadership experience or administrative potential, protected leadership opportunities are available in areas including quality, patient safety, clinical operations, and program development.
NewAnesthesiology - Vice Chair of Research Cedars-Sinai Health SystemAnesthesiology - Vice Chair of ResearchLos Angeles, CA$545,896–$714,043 / yearThe total pay range shown takes into account the wide range of factors that are considered in making compensation decisions including knowledge/skills; relevant experience and training; education/certifications/licensure; and other business and organizational factors. Cedars-Sinai Medical Center, a state-of-the-art, 958 bed tertiary acute care academic medical center is committed to excellence in compassionate patient care, research, education, and community programs to improve the lives of our patients.
NewBRCA Center Director Cedars-Sinai Health SystemBRCA Center DirectorLos Angeles, CA$400,000–$682,000 / yearIn cooperation with leadership, draft and deploy a strategic plan for the center required to support the successful development of a nationally recognized and extramurally funded research and clinical program of excellence for BRCA cancers, including talent, space, and financial requirements. Proven administrative and organizational leadership: Track record of administrative accomplishment, including leading interdisciplinary teams and oversight of departments, centers, and/or institutes; able to translate strategy into measurable outcomes.
Senior Specialist, Clinical Education, Clinical Development Edwards LifesciencesSenior Specialist, Clinical Education, Clinical DevelopmentIrvine, CaliforniaRepresent TMTT during complex research cases (ESAPCU, clinical trial, commercial) with investigating physicians, hospital staff and clinical research coordinators by providing on-site, real-time guidance during implants, including contingency planning to address unforeseen occurrences in support novel devices. This role partners cross-functionally with physicians, R&D, and commercial teams to support complex cases, develop procedural techniques, and translate real-world clinical insights into next-generation device and therapy improvements.
Senior Specialist, Clinical Education Imaging, Clinical Development Edwards Lifesciences CorpSenior Specialist, Clinical Education Imaging, Clinical DevelopmentIrvine, CA$134,000–$190,000 / yearRepresent TMTT during complex research cases (ESAPCU, clinical trial, commercial) with investigating physicians, hospital staff and clinical research coordinators by providing on-site, real-time imaging and clinical guidance during implants, including contingency planning to address unforeseen occurrences in support novel devices. What you'll need (Required): Bachelor's Degree in biological or life sciences, animal science, or other related scientific or technical field with 5 years experience of independent echo sonography scanning in a clinical setting or equivalent work experience based on Edwards criteria.
Clinical Research Coordinator II National InstituteClinical Research Coordinator IIGarden Grove, California$24–$32 / hourNICR provides sponsors and CROs premium services leading to rapid study site identification, trial placement, site initiation, and successful subject enrollment. Who We Are From our roots in Nephrology, we have expanded into many other specialty fields, including cardiometabolic, infectious diseases, geriatrics, and many other challenging & underserved areas of healthcare.
Senior Clinical Research Coordinator National InstituteSenior Clinical Research CoordinatorHuntington Beach, CaliforniaPerform or provide direct oversight of Clinical Research Coordinator responsibilities, including subject visits, informed consent, source documentation, investigational product accountability, data entry, query resolution, scheduling, specimen processing, and sponsor communication when necessary to support site operations. Additionally, you will formally supervise, support, and mentor clinical staff—including Coordinators, Principal Investigators, and Sub-Investigators—to optimize patient flow and deliver exceptional performance.
BCBA Clinical Supervisor Easterseals Southern CaliforniaBCBA Clinical SupervisorNorthridge, CaliforniaCompetent in employing and directing behavior analytic methodologies including Pivotal Response Training (PRT), Natural Environment Teaching (NET), Picture Exchange Communication System (PECS), Behavior Skills Training (BST), and Experimental Functional Analysis (EFA). OVERVIEW OF POSITION: Under direct supervision, provides quality clinical supervision and work direction to direct reports, providing discipline- specific treatment for children with developmental delays, disabilities, and autism spectrum disorders (ASD).
Senior Clinical Research Coordinator National Institute of Clinical Research, Inc.Senior Clinical Research CoordinatorHUNTINGTON BEACH, CA$28–$40 / hourFull timePerform or provide direct oversight of Clinical Research Coordinator responsibilities, including subject visits, informed consent, source documentation, investigational product accountability, data entry, query resolution, scheduling, specimen processing, and sponsor communication when necessary to support site operations. Technical Proficiency: Highly proficient in using Clinical Trial Management Systems (CTMS), Electronic Data Capture (EDC) systems, and electronic Trial Master Files (eTMF).
Clinical Research Recruitment Coordinator Irvine Clinical ResearchClinical Research Recruitment CoordinatorIrvine, CAIrvine Clinical Research is looking for a friendly, outgoing person to join our team as a Clinical Research Recruitment Coordinator. Recruit study participants via short telephone interviews; make outbound phone calls to achieve appointment scheduling goal.
Clinical Research Coordinator (Experienced) - Westside Los Angeles Irvine Clinical ResearchClinical 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 Research Coordinator (Experienced) - San Gabriel Valley Irvine Clinical ResearchClinical Research Coordinator (Experienced) - San Gabriel ValleyArcadia, CA$30–$40 / hourFull timeFinal hourly 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.
Clinical Research Coordinator (Experienced) - Long Beach Irvine Clinical ResearchClinical 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.
Mobile Clinical Research Nurse - Chatsworth, CA Vita MobileMobile Clinical Research Nurse - Chatsworth, CAChatsworth, CAVitaMobile Medical Support Services has an urgent need for a per diem Registered Nurse to join our Clinical Research Team as a Mobile Clinical Research Nurse. Study visit activities include, but are not limited to: Scheduling visits with study participants.
Specialist, Clinical Research Edwards LifesciencesSpecialist, Clinical ResearchIrvine, California$87,000–$123,000 / yearBachelor's Degree in Life Sciences or Nursing with 3 years of experience in clinical research (site management, clinical project management, monitoring, and/or CRC) including quality assurance/control and regulatory compliance or field monitoring with experience in the healthcare industry or equivalent work experience based on Edwards criteria. Conducting in-house and site (if applicable) reviews of associated documentation and participate in internal and competent authority (e.g., FDA, DEKRA, PMDA) audits to ensure all essential clinical Trial Master File (TMF) documents are compliant with Good Documentation Practices, Edwards internal SOPs, and US and OUS regulations.
Manager, Clinical Case Review Edwards LifesciencesManager, Clinical Case ReviewIrvine, CAThe Case Review Manager leads the patient screening analysis and evaluation of baseline medical history and clinical imaging reports (e.g EDC screening records including clinic notes, lab results, cardiology assessments, CT and/or echocardiogram reports) to confirm protocol compliance and provide patient screening and case review support to clinical trial sites for Clinical Research Trials within THV Clinical Affairs. + Previous related experience working a clinical setting or equivalent work experience based on Edwards criteria Preferred and Experience working in the setting of a clinical trial or equivalent work experience based on Edwards criteria Preferred.
Founding Product Engineer - Clinical Systems RDIFounding Product Engineer - Clinical SystemsLos Angeles, CaliforniaWe already have working internal products, real clinical workflows, real users, and a clear list of problems worth solving. Engineers sit close to the business, close to users, and close to the consequences of what they build.
Director, Clinical Affairs Saluda Medical Pty LtdDirector, Clinical AffairsCAWhat Youll Do: Development, maintenance, and optimization of the clinical quality system, clinical regulatory requirements, and data integrity/quality Establish detailed program plans, drive program execution toward established objectives, assess risk and implement strategies to ensure successful delivery of the clinical objectives Contribute to the overall strategic direction for development and implementation of clinical affairs objectives and processes Direct and collaborate with internal and external staff to assure successful conduct of assigned clinical programs consistent with company objectives and applicable regulations and policies Development of protocols, statistical analysis plans, reports and other clinical study documentation Support and contribute to manuscripts, abstracts, data presentations, and health economic value initiatives Promote and embody culture and behavior expectations of a high-performance culture Drives leadership of issue identification and resolution. Knowledge/Skills/Abilities: Excellent verbal and written communication Ability to think creatively, dynamically, and foster a culture of commitment to thoughtful science to help patients in need Knowledge of ICH/GCP and FDA medical device regulations Knowledge of electronic data capture systems and web-based clinical trial management tools Knowledge of research design, data analysis and biostatistics Self-motivated and independent work style with the ability to initiate and follow through on assignments Self-assured, knowledgeable professional capable of developing good interpersonal relationships with medical professionals Excellent organizational skills and attention to detail High degree of personal integrity.