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The Director, Clinical Data Management will be responsible for daily data management tasks for all phases of clinical trials including CRO oversight and support other functional areas such as clinical operations, statistical programming, biostatistics, and medical monitor.
$242,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Two (2) years clinical experience as a Radiologic Technologist in an acute care medical center 6 months of clinical experience as a Magnetic Resonance Imaging Technologist in an acute care medical center.
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Develop manufacturing plans with resources and supervise schedules to meet clinical demand and new clinical trials on both the cell therapy and/or exosome platforms. Directly oversee the manufacturing of product candidates for early stage and late-stage clinical trials.
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By coordinating and promoting scientific research and exchange within the academic community, as well as providing clinical resources and education to the community at large, THI strives to halt the spread of HIV through cutting-edge research, innovative clinical trials, compassionate care, and public education.
$224,200 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Must have current Clinical Laboratory Scientist (CLS) or appropriate sub-specialty license issued by the State of California, Department of Public Health or CHS (Clinical Histocompatibility Scientist License.
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Familiarity with regulatory requirements for clinical trials, including IRB submissions and reporting processes. Our core practice areas include vaccine research, development, and production; microbiology and infectious disease research; biodefense; clinical research; global health security; and HIV/AIDS programs.
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Must be licensed as a Licensed Clinical Psychologist, Licensed Marriage and Family Therapist (LMFT), Licensed Clinical Social Worker (LCSW) or Licensed Professional Counselor (LPC) Therapist community: Work in private practice without feeling like you’re on an island.
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The Clinical Trials Office (CTO) is an integral component of the Stanford Cancer Institute since the vital work performed there enables our adult and pediatric cancer centers to translate research from the laboratory into the clinical setting.
$126,000 a yearPart-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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SOME OF OUR SWEET SHIFT LEADER PERKS:Flexible part-time work schedulesPay-on-Demand (no longer do you have to wait until the end of the week. plus tipsPaid vacation and sick time offInteractive training & mentorshipPet insurance for your furry loved onesJob stability with a rapidly growing and reputable companyAchievable growth/promotion opportunitiesYou get to work in a fun, exciting team environmentEmployee discount and FREE cookies with every shift.
$18.3 an hourFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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As mandated by the State of California, those employees who work at Residential, Outpatient, Sober Living, provide Mental Health Services, Administrative Staff or Transitional Living Facilities must be fully vaccinated and have received a booster.
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The primary responsibilities will involve the isolation of primary lymphocytes for pre-clinical research, CAR-T cell production, characterization of various products using flow cytometry and other in-vitro assays, along with scheduling and management of several direct reports.
$120,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Work collaboratively with computational biology group to integrate complex data sets including epigenomic and other ‘omic’ data in pre-clinical settings for target discovery, validation, and advance mechanism of action target biology.
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Reporting directly to the Disease Team Project Manager, the Clinical Research Coordinator I is responsible for coordinating and managing clinical trials including providing all aspects of protocol management, including screening for patient eligibility, data collection and analysis, ensuring protocol compliance, adverse drug reaction reports, monitoring patient treatment and toxicities, laboratory and specimen submission, and maintenance of accurate and complete clinical research files.
$51.44 an hourFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Unlike CAR-T and any genetically modified cell therapy, AlloNK has not shown any secondary malignancies in our clinical trials, which is a benefit in an autoimmunity setting. AlloNK is currently being evaluated in combination with B-cell targeted mAbs in patients with autoimmune diseases and cancers, such as lupus nephritis, SLE, rheumatoid arthritis, pemphigus vulgaris, the ANCassociated vasculitis subtypes GPA/MPA, and B-NHL. In addition, we are also pursuing AlloNK and our CAR-NK product candidates in multiple indications through collaborator-funded trials.
$230,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Current IBCLC Certification OR previous IBCLC Certification with 10 years of clinical lactation experience. Job DescriptionThis is a Casual/Per-Diem position with a 12-hour night shift schedule on variable days of the week including weekends and holidays.
$57 - $81.6 an hourExpandApply NowActive JobUpdated Today
clinical trials shift work jobs Company: Emory University in San Diego, CA
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