Senior Analyst, Clinical Data Management Edwards LifesciencesSenior Analyst, Clinical Data ManagementIrvine, CaliforniaLeading project management activities for multiple (multi-site and multi-cohort) projects to bring clinical studies on-line, including conducting project team meetings, establishing and maintaining project timelines, and communications to stakeholders. Defining and specifying clinically complex data collection requirements (e.g., eCRFs, CRFs, edit checks and collection of external data) for assigned studies; including defining, performing, and coordinating user acceptance testing (e.g.
Assay Development Research Scientist I Fulgent Genetics IncAssay Development Research Scientist IEl Monte, CAContinually assess and integrate cutting-edge technology into our laboratory and development process, our Assay Development - Research Scientists will play a key role in developing new tests as well as troubleshooting and maintaining existing assays. Search firms or agencies without an applicable contract and/or express approval to recruit for the role in question - that choose to submit a resume or client information to our career page or to any employee of Fulgent - will not be eligible for payment of any fee(s), and any associated shared data will become the property of Fulgent.
Engineering Technician, Research & Development Process & Product Design Alcon ResearchEngineering Technician, Research & Development Process & Product DesignLake Forest, CaliforniaIn this role, a typical day will include: Providing hands-on technical support for product design and development processes by assisting in testing, documentation, and compliance activities, ensuring accurate documentation of test results. Preferred Qualifications: Prior engineering or engineering technician experience, specifically in testing, product design, fixture development, and product assembly/rework support, ideally for medical devices.
Supervisor - Research Department Providence St. Joseph HealthSupervisor - Research DepartmentOrange, 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. These amounts are the base pay range; additional compensation may be available for this role, such as shift differentials, standby/on-call, overtime, premiums, extra shift incentives, or bonus opportunities.
Supervisor - Research Department Providence Health & ServicesSupervisor - Research DepartmentOrange, CARequsition ID: 452523 Company: Providence Jobs Job Category: Research Job Function: Clinical Support Job Schedule: Full time Job Shift: Day Career Track: Leadership Department: 7520 RESEARCH PROJECTS CA HERITAGE SERVICES Address: CA Orange 1100 W Stewart Dr Work Location: St Joseph Hospital-Orange Workplace Type: On-site Pay Range: $47.05 - $73.04 Together, 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.
Research Assistant (Bilingual-Spanish) - Riverside Irvine Center for Clinical Research IncResearch Assistant (Bilingual-Spanish) - RiversideRiverside, CAIdeally, candidates will have prior healthcare, clinical, or laboratory experience, with a passion for assisting coordinators with participant visit workflows, sample processing, and administrative support while producing quality work. Front Desk & Reception Management: Serve as the primary point of contact at the front desk; warmly greet participants, study partners, and visitors; manage participant check-in/check-out; and handle incoming clinic phone calls.
Postdoctoral Scholar - Research Associate - Cancer Genomics and Therapeutics University of Southern CaliforniaPostdoctoral Scholar - Research Associate - Cancer Genomics and TherapeuticsLos Angeles, CAWhen extending an offer of employment, the University of Southern California considers factors such as (but not limited to) the scope and responsibilities of the position, the candidate's work experience, education/training, key skills, internal peer equity, federal, state, and local laws, contractual stipulations, grant funding, as well as external market and organizational considerations. Responsibilities include a) Processing and analyses of clinical samples, b) Conducting cellular, molecular, and in vivo experiments for hypothesis-driven research, c) Performing computational and bioinformatic analyses; and d) Preparing presentations and publishing scientific manuscripts under the direction of the Principal Investigator.
Research Associate CRESCENTA BIOSCIENCES INC.Research AssociateIrvine, CAFull timeThe successful candidate will perform and support laboratory studies evaluating small-molecule drug candidates, working closely with senior scientists and company leadership. This position is particularly well suited for a scientist who enjoys hands-on experimental work while taking ownership of laboratory operations in a dynamic, collaborative biotechnology environment.
Research Coordinator II University of Southern CaliforniaResearch Coordinator IILos Angeles, CA$35.53–$46.59 / hourWhen extending an offer of employment, the University of Southern California considers factors such as (but not limited to) the scope and responsibilities of the position, the candidate's work experience, education/training, key skills, internal peer equity, federal, state and local laws, contractual stipulations, grant funding, as well as external market and organizational considerations. The Department of Psychiatry and Behavioral Sciences at the Keck School of Medicine of USC is seeking a detail-oriented and highly motivated Research Coordinator II to support clinical trials and observational research in Alzheimer's disease, related dementias, and neurodegenerative disorders.
Research Coverage Analyst - Remote Providence Health & ServicesResearch Coverage Analyst - RemoteCalifornia, CARemoteRequsition ID: 453732 Company: Providence Jobs Job Category: Research Job Function: Clinical Support Job Schedule: Full time Job Shift: Day Career Track: Clinical Professional Department: 4007 SS OFFICE OF RESEARCH ADMINISTRATION Address: WA Spokane 101 W 8th Ave Work Location: Sacred Heart Medical Center-Spokane Workplace Type: Remote Pay Range: $See Posting - $See Posting The amounts listed are the base pay range; additional compensation may be available for this role, such as shift differentials, standby/on-call, overtime, premiums, extra shift incentives, or bonus opportunities. Main responsibilities include completing a comprehensive Medicare Coverage Analysis in alignment with Medicare''s Clinical Trial Policy, national medical guidelines, local practice guidelines, peer-reviewed publications and local and national coverage determinations that encompasses all billable services within the clinical trial protocol.
Research Assistant - Long Beach Irvine Center for Clinical Research IncResearch Assistant - Long BeachLong Beach, CAOur 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. Healthy Brain Clinic in Long Beach, CA is part of the Irvine Clinical Research site network, the largest of its kind on the West Coast.
Sr. Research Associate, Analytical Development Avid Bioservices IncSr. Research Associate, Analytical DevelopmentTustin, CA$84,000–$105,000 / yearResearch Associate, you'll have the opportunity to focus on developing Cell-based, ELISA, HPLC, CE, PCR and/or SDS-PAGE methods, and you'll work alongside experienced analytical scientists and process development scientists to identify and characterize protein biologics. Avid Bioservices is a leading clinical and commercial biologics CDMO focused on creating innovative solutions to meet the needs of our clients and improve patient outcomes.
Sr. Research Associate, Process Development Upstream Avid Bioservices IncSr. Research Associate, Process Development UpstreamTustin, CA$72,800–$91,000 / yearWork with many different kinds of mammalian cell lines (CHO-GS, CHO-DG44, CHO-M, CHO-S, NSO, HEK, etc) utilizing aseptic techniques, and apply a good understanding of the effect of general metabolic pathways (nutrient usage, expression system, etc.) physical (morphology, pH, osmolality, etc.) as well as mechanical (agitation speeds, oxygen and pH control, etc.) parameters on cell growth and recombinant protein production. Analyze growth, production and nutrient usage data, create data spreadsheets and graphs in Excel or JMP, document data and findings for traceability and regulatory requirements, write technical and summary reports, generate slide decks, and lastly, communicate findings and participate in scientific discussions within the group and with clients.
Sr. Research Associate, Process Development Downstream Avid Bioservices IncSr. Research Associate, Process Development DownstreamTustin, CA$72,800–$91,000 / yearMinimum Qualifications: Bachelor's degree with 3-4 years of relevant biopharmaceutical industry experience, or a Master's degree in Chemical Engineering, Biochemical Engineering, Biotechnology, Biological Sciences, or a related field. Avid Bioservices is a leading clinical and commercial biologics CDMO focused on creating innovative solutions to meet the needs of our clients and improve patient outcomes.
Research Associate, Analytical Development Avid Bioservices IncResearch Associate, Analytical DevelopmentTustin, CA$31.15–$38.94 / hourYour focus will be to develop Cell-based, ELISA, HPLC, CE, PCR and/or SDS-PAGE methods, and you'll have the chance to interface with Quality Control as methods are transferred into that group for cGMP testing. Physical Demands & Work Environment: In this dynamic role, expect a blend of regular activities like sitting, standing, and walking, with occasional physically engaging tasks such as lifting objects up to 25 pounds.
Research Compliance Analyst III Tulane UniversityResearch Compliance Analyst IIILa, CAPreferred Qualification: Juris Doctorate or other advanced degree, or a combination of Bachelor's Degree with three to five years of experience working in human subjects research either in the capacity as a researcher or research management. Minimum Qualification: Bachelor's Degree and three (3) years of human subjects clinical research experience, including legal and/or regulatory research experience.
(Senior) Medical Science Liaison, External Research Tempus AI Inc(Senior) Medical Science Liaison, External ResearchCARemote$120,000–$190,000 / yearSupport the development and management of a Medical Research Strategy and Scientific Exchange Plans to guide the prioritization of new external research investments through conducting biannual clinical reviews of unmet needs for biomarkers for immunotherapy and targeted therapies, tumor response monitoring, and minimal residual disease in each cancer type. Engage academic KOLs and investigators in oncology to work on collaborative external research with Tempus, including investigator-initiated trials, assay grants for biobank samples or prospective trials, and real-world retrospective data studies.
Spec 1, Clinical Operations TechDigital CorporationSpec 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. Job Description: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.).
Wetlab Supervisor, Surgical Training Research & Development Process & Product Design Alcon IncWetlab Supervisor, Surgical Training Research & Development Process & Product DesignLake Forest, CAPrimary responsibilities will include but are not limited to; supporting design and development activities on R&D Projects, organizing and prioritizing competing objectives, assigning and following up on assigned tasks, reviewing and approving timesheets, participate and/or coordinate Pre-Clinical and/or Simulated Use Wet Labs. The R&D Lab Supervisor must be able to partner with R&D Leadership and/or project engineers to understand project priorities and deliverables to ensure the right skillsets are selected or hired to ensure project deliverables and tasks are completed correctly and on time.
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.