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Prior experience in providing MSL-level support to products or devices in endocrinology and/or rare disease, including KOL development, investigator-initiated clinical trials, publications and educational programs, highly preferred.
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At Cedars-Sinai Cancer, we offer state-of-the-art treatments, experimental therapies, next-generation research, and cutting-edge clinical trials for over sixty types of cancer at more than ten locations throughout Greater Los Angeles.
$850,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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The AC has a four-part mission to: (a) advance and support clinical trials and therapeutic development for cell and gene therapies; (b) engage diverse and underserved communities in those trials and the resulting therapies; (c) provide training and education to researchers, staff, patients, and communities; and (d) exchange novel expertise with other AC network sites through lead offerings.
$20.93 an hourPart-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Minimum Qualifications: 3+ year experience in clinical trial coordination with 1+ years pediatric clinical trials experience. Position Summary: As a member of the Bone and Soft Tissue Tumors team (BSTT), the Clinical Research Coordinator II will be responsible for managing multiple clinical trials of phases I through III in accordance with federal and local regulations.
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The PIE – Forensic Psychology Specialist will in addition, provide ongoing consultation and training around clinical legal testimony and how to prepare as the expert witness in both bench trials and jury trails.
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Primary duties will include: meeting with clients, drafting pleadings, administering depositions, propounding and responding to discovery, conducting research, writing motions, making court appearances, arguing motions, participating in trials, interviewing witnesses, drafting agreements, negotiating settlements, attending mediations, and arbitrations, handling Probate Litigation cases and other activities requested by the partners.
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RDI is seeking a Clinical Trial Manager to be responsible for executing trials from start to finish. Provide clinical trial expertise and oversight to team of Project Assistants and Lab Assistants.
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Minimum Qualifications Must be a Licensed or License-Eligible Marriage and Family Therapist (MFT/LMFT), Clinical Social Worker (MSW/LCSW), or Professional Clinical Counselor (APCC/LPCC.
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Req Knowledge of basic computer skills including Microsoft Office applications Preferred Qualifications: Pref Clinical Laboratory Specialist in Microbiology (ASCP) Required Licenses/Certifications: Req Clinical Laboratory Scientist - CLS OR Limited license from the State of California.
$76.07 an hourPart-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Licensed or certified by the California Department of Public Health as a Clinical Laboratory Scientist, Limited Clinical Laboratory Scientist, Clinical Microbiologist Scientist, or Public Health Microbiologist.
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Opportunity for leadership positions - Lead CRA, CRA Manager, Clinical Trial Manager, Training and Development Manager, and many more; On-site and virtual/remote monitoring activities with a risk-based monitoring approach (including centralized data review) through our integrated Clinical Trial Management System to identify site deviations/deficiencies and corrective/preventive actions to bring a site back into compliance and mitigate risks moving forward.
$160,000 a yearFull-timeWork from homeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Registered with the Board of Behavioral Sciences as an Associate Clinical Social Worker (ASW) or Associate Marriage and Family Therapist (AMFT) Minimum of 2 years of providing human services to a special needs’ population, including at least 1 years of complex clinical experience in homelessness, addictions, under-served population, or prison re-entry/diversion program.
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Assists with clinical trial budgets. The Clinical Research Associate I works directly with a Clinical Research Coordinator, Research Program Administrator, or Research Nurse to coordinate and/or implement the study.
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The Risk Adjustment Coder is responsible for evaluating the accuracy and consistency of coded clinical data quality results and reports in accordance with all applicable federal, state and county regulations/laws related to coding, auditing, and clinical documentation guidelines for the various risk adjustment models.
$28.15 an hourFull-timeExpandApply NowActive JobUpdated 30 days ago - UpvoteDownvoteShare Job
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The lab also participates in national trials using brain stimulation (e.g., transcranial magnetic stimulation (TMS. Technical knowledge of neuroimaging and brain anatomy, experience with organizing, maintaining, and analyzing large brain imaging datasets, programming expertise with python, Bash and parallel computing, experience with Brain Imaging Data Standards (BIDS) and MRI—based neuroimaging software programs (e.g., FreeSurfer, ITKSna) and statistics/machine learning strongly preferred.
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clinical trials jobs Title: trial master in Los Angeles, CA
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