Director, Clinical Operations COPE HEALTH SOLUTIONSDirector, Clinical OperationsLos Angeles, CA$172,100–$211,575 / yearOur comprehensive NCQA certified population health management platform and highly experienced team brings deep expertise, experience, proven tools, and processes to improve financial performance and quality outcomes for all types of payers and providers. Minimum of 5-10 years of progressive clinical experience, including significant leadership or management experience in clinical operations, quality assurance, or healthcare program management.
Data Analyst - Biorepository Operations City of HopeData Analyst - Biorepository OperationsDuarte, CAInform Research Informatics on new users and iLab-related workflow enhancements at an agreed cadence; prepare and execute weekly, monthly, and annual metrics/status reports; monitor data and provide dashboards and updates; validate user requirements as software iterations are built. Youll partner with biorepository staff, researchers, vendors, and Research Informatics to strengthen data quality, streamline workflows, and expand system capabilities so biospecimens are received, tracked, reported, and shipped accurately across sites.
Clinical Operations Manager BetterHelpClinical Operations ManagerCA$85,000–$100,000 / yearWe only post open roles on our career page (betterhelp.com/careers) or reputable job boards like our official LinkedIn or Indeed pages, and all official BetterHelp recruitment emails will come from the domain @betterhelp.com. With your experience and opinions from direct clinical care, you are confident in your abilities to apply the best of "what's working today" in the mental healthcare system, while being a vocal proponent of what "red tape" should be eliminated or redesigned to better serve clients and their therapeutic progress.
Mgr, Clinical Operations (RN) - Inservice Education MemorialCare Health SystemMgr, Clinical Operations (RN) - Inservice EducationLong Beach, CA$75.25–$117.36 / hourPrimary Location: United States-California-Long Beach Job: RN House Supervisor, Unit Mgr Organization: Long Beach Memorial Medical Center Schedule: Full-time Employee Status: Regular Job Level: Manager Job Posting: Feb 28, 2026, 6:46:24 AM Work Schedule: 8/40 work shift hours Shift: Day Job Department Name: Inservice Education. Across our family of medical centers, we support each one of our bright, talented employees in reaching the highest levels of professional development, contribution, collaboration and accountability.
Mgr, Clinical Operations (Rn) - Inservice Education MemorialCare Health SystemMgr, Clinical Operations (Rn) - Inservice EducationLong Beach, CA$75.25–$117.36 / hourIn addition to base pay, there may be additional compensation available for this role, including but not limited to, shift differentials, extra shift incentives, and bonus opportunities. The incumbent shall plan, organize, direct and evaluate people and activities for the assigned unit(s) to ensure the delivery of high quality, cost effective patient care.
Senior Clinical Research Coordinator - Hematology/Oncology (Marina del Rey) University of CaliforniaSenior Clinical Research Coordinator - Hematology/Oncology (Marina del Rey)Marina del Rey, 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.
Senior Operations Manager Volunteers of America Los AngelesSenior Operations ManagerDowney, CA$95,000–$100,000 / yearPROGRAM DEVELOPMENT: In collaboration with the Clinical Regional Director and the Program Managers, develop and manage program budgets, programmatic and individual performance goals, and service delivery for SCADP programs in accordance with the various grant/contract/state requirements Develop program policies, procedures, plans, and associated communications needed to operate residential and non-residential programs serving various populations of underserved individuals. COORDINATE MULTIPLE PROGRAMS: With the Program Managers, supervise operations of multiple teams of staff engaged in various programs, collaborate with HR Department Corporate administration staff Address employee issues, coordinate with Regional Clinical Director and Program Managers all staffing issues, and employee conflicts, involve HR as required.
Clinical Data Manager Ambu A/SClinical Data ManagerCARemoteAs part of our growing Clinical Data Acquisition team, the Clinical Data Manager will play a critical role in generating the high-quality clinical data needed to support the development of Ambus next generation of AI-powered Endointelligence solutions. Unlike traditional pharmaceutical clinical trial roles, this position focuses on the planning, execution, and oversight of medical device clinical studies designed to acquire clinical data that supports product innovation, algorithm development, and clinical validation.
Director, Operations Support & Strategy Welbe HealthDirector, Operations Support & StrategyLos Angeles, CA$159,939.07–$211,119.57 / yearThe Director, Operations Support & Strategy partners closely with leaders across WelbeHealth to drive high-impact initiatives that improve our operational and clinical performance, with a focus on our strategic pillars and as directed based on specific work assignment. Through complex problem solving and analysis, effective stakeholder engagement, management process design, and a focus on simplicity and replicability, the Director, Operations Support & Strategy helps deliver measurable performance improvements as we grow.
Manager, Regulatory Labeling and Operations LivaNova PlcManager, Regulatory Labeling and OperationsCA$120,000–$145,000 / yearThe role ensures all labeling (IFU, packaging labels, e-labeling, and software UI text) is accurate, compliant, and aligned with global regulatory requirements, while also driving scalable processes across UDI, localization, and labeling operations. If you are concerned that an offer of employment might be a scam or that the recruiter is not legitimate, please verify by searching for "See Open Jobs" on https://www.livanova.com/en-us/careers , and check that all recruitment emails come from an @livanova.com email address.
Director of Operations SHPCA SCAN Health PlanDirector of OperationsLong Beach, California$147,900–$214,030 / yearHowever, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor’s legal duty to furnish information. Our work spans Medicare Advantage, fully integrated care models, primary care, care for the most medically and socially complex populations, and next-generation care delivery models.
Manager, Clinical Quality System Documents Arrowhead PharmaceuticalsManager, Clinical Quality System DocumentsLos Angeles, CA$120,000–$145,000 / yearLead and coordinate document activities with cross-functional business stakeholders, including Clinical Operations, Drug Safety/Pharmacovigilance, Biometrics, Clinical Data Management, Clinical Development/Medical, Regulatory Affairs, Medical Writing, Clinical Supply Management and Clinical Quality Assurance, ensuring timely completion of document deliverables. Support QMS Quality Assurance (QA) counterparts in executing document control workflows by coordinating and facilitating the development, review, revision, approval, issuance, periodic review, and retirement of controlled documents across Clinical Development functions, ensuring timely completion and compliance with established document control processes.
Medical Assistant/JR Clinical Research Coordinator National InstituteMedical Assistant/JR Clinical Research CoordinatorPomona, CaliforniaNational Institute of Clinical Research, a research organization serving the pharmaceutical and biotech industries, is searching for a highly experienced Medical assistant with Phlebotomy experience to assist our research coordinators in clinical trials. Essential functions include scheduling research visits for subjects enrolled in clinical trials, the performance of EKG, routine phlebotomy, other lab assessments such as vital signs, and obtaining necessary lab results for the subjects.
NewCardiac ICU Clinical Supervisor MemorialCare Health SystemCardiac ICU Clinical SupervisorLong Beach, CA$66.32–$99.47 / hourDemonstrates positive, professional communication with patients, families, physicians, departmental and interdepartmental staff to optimize workflow and to facilitate problem identification and resolution. Provides ongoing assessment of department operations and patient care processes for opportunities to improve, facilitates data collection and participates in quality activities to improve care.
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.
Assistant Professor/Clinical Coordinator Charles R. Drew UniversityAssistant Professor/Clinical CoordinatorLos Angeles, CaliforniaCarry a fair share of other duties (department and committee work, curriculum development, course revision, community outreach, program planning and review, attending advisory meetings, assessing and improving student learning outcomes).PC proficient in MS Office (Word, Excel, PowerPoint, Outlook, etc.). Evidence of prior college-level instruction and supervision of radiologic technology students in a Joint Review Committee on Education in Radiologic Technology (JRCERT)-accredited program.
Clinical Research Coordinator II National InstituteClinical Research Coordinator IIGarden Grove, California$24–$32 / hourNICR combines the use of the latest technologies, streamlined clinical operations, and extensive access to a diverse population to deliver the highest quality clinical trials for life-changing therapies. NICR provides sponsors and CROs premium services leading to rapid study site identification, trial placement, site initiation, and successful subject enrollment.
Clinical Research Coordinator I, Oncology Children's Hospital of Orange CountyClinical Research Coordinator I, OncologyOrange, CaliforniaStudy management includes but is not limited to assisting in assessing feasibility of clinical research protocols, preparing materials needed for regulatory review and submission to the Institutional Review Board (IRB), identifying potential study participants, 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. 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 Physical Activity Lifting .
NewClinical Research Coordinator Avispa Fukuoka Co LtdClinical Research CoordinatorLos Angeles, CACollaborate with investigators, sponsors, monitors, and research teams to support Phase I-IV, industry-sponsored, investigator-initiated, NIH-sponsored, interventional, observational, multicenter, and academic medical center research studies. Clinical Research Coordinator Responsibilities: Oversee daily operations of multiple clinical research studies, ensuring compliance with sponsor, institutional, FDA, GCP, and regulatory requirements throughout study start-up, maintenance, monitoring, and close-out activities.
Project Manager - Clinical Projects - Torrance Project Management · Torrance, CA PolyPeptide Laboratories IncProject Manager - Clinical Projects - Torrance Project Management · Torrance, CATorrance, CA$85,000–$105,000 / yearYou 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.