Senior Clinical Systems Engineer (Medical Device Integration) - Hybrid Cedars-Sinai Medical CenterSenior Clinical Systems Engineer (Medical Device Integration) - HybridLos Angeles, CACuriosity, diligence, follow-through, and critical thinking are hallmarks of this high functioning team who research, design, develop, and deliver clinical technology solutions that including databases, interfaces, edge device messaging. What will you be doing: The Senior Clinical Systems Engineer is a highly visible role that collaborates with Clinical Operations, Technology Teams, Application Teams, and vendors to deliver and optimize integrated clinical solutions.
Portfolio Clinical Leader Pennant Group IncPortfolio Clinical LeaderCA$120,000–$150,000 / yearResponsible for the recruitment, orientation, onboarding, and ongoing leadership development of key clinical leaders within the market's agencies, in collaboration with the agency's Executive Director with the ultimate goal of clinical leaders become C-level owners. Time management and organizational skills necessary to manage multiple projects, appropriately prioritize workload, plan for agency leader's to meet deadlines and goals, and work independently in responding to day-to-day functional needs.
Spec 1, Clinical Operations MillenniumSoft IncSpec 1, Clinical OperationsIrvine, CAEnsure compliance with regulations and manage the lifecycle of devices, while closely partnering with other internal key stakeholders ( e.g., clinical study teams, Manufacturing Operations, Finance, Supply Chain, Quality, and Compliance groups) to develop and lead the execution of the device process, and ensuring continuous process improvement of efficiency and accuracy of processes and procedures. Identify, develop, recommend, and implement, moderately complex process development and process improvement solutions to optimize global trial workflow timelines, (e.g., device return aging issues, status of open device issues/queries, etc.).
Senior Clinical Engineer - Onsite Cedars-Sinai Medical CenterSenior Clinical Engineer - OnsiteLos Angeles, CAWhat will you be doing in this role: The Clinical Engineer III provides engineering services to medical and research areas including: selection, acquisition and service of medical devices, project management, technical investigations of clinical incidents, clinical/technical problem-solving, system design, and solution of novel system and technical problems. Responsible for moderate to the most complex equipment management by working with a multidisciplinary team of internal and external customers and stakeholders to identify needs, coordinates purchases, manages installations, organizes in-service trainings, plans for the handoff to day-to-day operations, and documents projects.
NewDirector, Clinical Trial Portfolio Management CG Oncology IncDirector, Clinical Trial Portfolio ManagementCARemoteThe ideal candidate has demonstrated experience supporting registrational and lifecycle clinical programs in biotechnology or pharmaceutical environments, partnering with cross-functional leaders, supporting global health authority readiness, managing integrated plans, risks, governance forums, budgets, and submission-readiness milestones, and translating long-range strategy into disciplined execution over a multi-year planning horizon. The Director, Clinical Trial Portfolio Management is a senior program and portfolio management leader within the PMO function, responsible for developing and maintaining the integrated portfolio view across clinical programs and cross-functional workstreams required to deliver the clinical, registrational, and lifecycle strategy.
Division Chair, Applied Clinical Psychology The Community SolutionDivision Chair, Applied Clinical PsychologyLos Angeles, LouisianaManaging the operations of the program in a complex, fast-paced higher education environment; Ensuring the quality of the faculty, curriculum, assessment of student learning, and scholarly activity of faculty and students. Founded in 1979 by a group of psychologists and educators, The Chicago School has grown into a dominant and globally respected leader in the fields of psychology and behavioral health sciences.
Clinical Scientist VesyncClinical ScientistTustin, CaliforniaThis role combines hands-on scientific and clinical support to the Behavioral Science (BeSci) team with the ownership of two external-facing functions: building and managing Clinical Research partnerships, and establishing and coordinating a Clinical Advisory Board. Intervention Content Development & Validation: In partnership with the Content team, support intervention content development and validation — ensuring content is clinically accurate, has the appropriate claims citations, appropriately nuanced, and calibrated to the right level of health literacy.
Clinical Dietitian Hybrid Compass Group North AmericaClinical Dietitian HybridCulver City, CA$75,000–$78,000 / yearCompass Group employs over 3,000 RDNs across the United States, making us one of the nation's largest employers of Dietitians in a variety of settings: Hospitals and healthcare systems. The company has earned significant recognition, including being named one of Modern Healthcare's "Top 100 Best Places to Work in Healthcare" for five consecutive years, and appearing on Training Magazine's Top 125 Organizations list for six straight years.
Study Project Manager II AbbVie IncStudy Project Manager IIIrvine, CALeadership: Demonstrates skills, experience and critical thinking to lead cross functional teams with minimal supervision; demonstrating expertise in end-to-end clinical study operations management (all phases, set up to close out) to drive milestone achievement. Coaching: contributes to Specialized Clinical Operations culture of supporting growth; Coaches and mentors team members, delegates and empowers to the right level, shares lessons learned, best practices and influencing skills training.
Site Manager ECN Operating LLCSite ManagerNorthridge, CAThe Site Manager reports directly to the assigned Regional Site Manager and is responsible for the deployment, oversight, and maintenance of Elite Clinical Network (ECN) processes in the conduct of clinical trials. The Site Manager oversees site staff, coordinates resources, monitors key performance indicators, and fosters a high-performing, patient-centric research environment.
Security Operations Analyst Anduril Industries IncSecurity Operations AnalystCosta Mesa, CA$129,000–$171,000 / yearProactively collaborate with a wide range of stakeholders, guiding detection and response maturity of key worlds, leading incidents and large-scale data baselines, and being responsible with mentoring and guiding junior analysts. To ensure your safety and help you navigate your job search with confidence, please keep the following critical points in mind: No Financial Requests: Anduril will never solicit payment or demand personal financial details (such as banking information, credit card numbers, or social security numbers) at any stage of our hiring process.
Director Medical Science Liaison Plastics & Regenerative Medicine AbbVie IncDirector Medical Science Liaison Plastics & Regenerative MedicineLos Angeles, CAThe Medical Science Liaison (MSL) Director for the Plastics & Regenerative Medicine team is a "player-coach" role responsible for providing leadership, strategic direction, and day-to-day operational management of a 6-person MSL team, while simultaneously maintaining an active field presence as the primary MSL for a small, dedicated territory (exact geography TBD). Provide expertise and feedback to coach MSLs in their most important activities (including engagement planning, ensuring that EE/HCP interactions are of high quality in scientific content and interaction approach (Challenger) and scientific storytelling, clinical study engagement activities, responding to medical information enquiries, capturing and reporting of data points and observations, coordination of activities with other in field teams).
Claims Clinical Specialist Genworth Financial IncClaims Clinical SpecialistCAYou will be responsible for communicating with medical personnel at Long Term Care Facilities, Home Care Agencies, and/or individuals by conducting telephonic assessments for claimants to develop the plan of care and provide tax qualified certifications as required by the policy. At least two years' experience working in a role that required an understanding of single and cumulative medical conditions (particularly those common in the aging process), including their effect on physical/cognitive function, as well as their prognosis and rehabilitative potential.
Project Manager, Medical Policy Processes Evolent Health IncProject Manager, Medical Policy ProcessesCAWhat You'll Be Doing: As a Project Manager on the Medical Policy team, you will work closely with Medical Policy teammates and other key stakeholder business groups to provide exceptional support of timely and accurate delivery of high-quality Evolent clinical guidelines. Technical Requirements: We require that all employees have the following technical capability at their home: High speed internet over 10 Mbps and, specifically for all call center employees, the ability to plug in directly to the home internet router.
Vocational Nursing Clinical Coordinator Stanbridge UniversityVocational Nursing Clinical CoordinatorIrvine, CA$90,000–$110,000 / yearInnovation and Technology: We embrace cutting-edge technology to enhance student learning through interactive, hands-on experiences, including virtual reality and simulation labs—ensuring students are prepared for the demands of modern healthcare practice. Sponsorship: Sponsorship now or in the future could include having Stanbridge University sponsor, complete employer documentation, provide attestations or training plans, or otherwise participate in a work-authorization or employment-based immigration program in order for an individual to begin or continue employment.
Quality Assurance Manager- Hybrid Sanguine BiosciencesQuality Assurance Manager- HybridLos Angeles, CaliforniaThis role is accountable for oversight and effectiveness of change control, Computer System Validation (CSV), including validation of GxP-relevant software, AI-assisted/low-code/no-code tools, and native-built applications, risk management, supplier/vendor quality, deviation/complaint handling, CAPA, internal auditing, and training. Oversee risk-based CSV activities for GxP-relevant software, spreadsheets, databases, workflow tools, AI-assisted applications, low-code/no-code solutions, and native-built applications, including intended use assessment, risk assessment, traceability, testing, deviation handling, and validation summary reporting.
Manager, Statistical Programming Arrowhead Pharmaceuticals IncManager, Statistical ProgrammingPasadena, CA$145,000–$160,000 / year4 years of relevant programming experience in pharmaceutical or biotechnology drug development; Proficiency in the use of statistical software including SAS, and familiarity of the use of R studio; Excellent verbal and written communication skills; Effective in communication and team collaboration, influencing across different functional lines; Understanding and experience with various aspects of a clinical development life-cycle, leading up to regulatory submission and post -approval activities; Experience interacting with and overseeing programming services of CRO vendors; and. As an internal expert in statistical programming, you will provide technical leadership and statistical programming input to closely collaborate with other functional teams at Arrowhead, including Clinical Development and Operations, Regulatory, Data Management, Medical Affairs, Program Management and others.
Medical Assistant- Certified Nursing Assistant- Pharm Tech Pasadena CA Profound Research LLCMedical Assistant- Certified Nursing Assistant- Pharm Tech Pasadena CAPasadena, CACoordinate with supervision duties for assigned clinical trials, including but not limited to study start-up, vendor management, subject recruitment, source document review and completion, protocol training, collection of regulatory documents, participant visits, timely data collection and documentation management, and reporting of adverse events, serious adverse events, and deviations, and monitoring visits and follow-up. Apply good documentation practices when collecting, maintaining, and correcting study data and required records of clinical trial activity, including but not limited to source documentation, case report forms, queries, drug dispensation records, and regulatory forms.
Manager of Global Project and Programs Business Excellence (Lake Forest, IL) AbbottManager of Global Project and Programs Business Excellence (Lake Forest, IL)Lake Forest, California$113,300–$226,700 / yearThe Manager, Production & Process Control, Global Business Excellence, leads strategic, cross-functional initiatives across the Core Laboratory Diagnostics Division to drive operational excellence, business performance, and margin improvement. This role partners with executive leadership to align programs with divisional priorities and leads Lean and Lean Six Sigma initiatives that deliver sustainable results across global operations.
Product Line Manager - Defense Electronics Manufacturing Teledyne TechnologiesProduct Line Manager - Defense Electronics ManufacturingTorrance, CA$140,000–$160,000 / yearThese markets include aerospace and defense, factory automation, air and water quality environmental monitoring, electronics design and development, oceanographic research, deepwater oil and gas exploration and production, medical imaging and pharmaceutical research. Background checks may include, but are not limited to, education verification, employment history and verification, criminal convictions, Motor Vehicle Report (MVR & driving history), reference check, credit checks/credit history and drug testing.