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The Clinical Research Coordinator I works independently providing study coordination, screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process.
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Master of Science in Nursing (MSN) with Clinical Nurse Specialist (CNS) The CNS reports to the Clinical Director and their designees in leading the nursing clinical practice and the advancement of excellence in patient care.
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Our Trial, White Collar and Investigations Business Unit boasts a diverse practice encompassing all facets of complex disputes, from pretrial resolution to trial, including business and commercial litigation, white collar defense and investigations, consumer protection and advertising, employment, entertainment, financial services litigation, health care litigation, intellectual property, patent litigation, and privacy and data security, among others.
$250,000 - $415,000 a yearFull-timeExpandApply NowActive JobUpdated 25 days ago - UpvoteDownvoteShare Job
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As business process owner within the Material Domain, The Supply Chain Manager is responsible for overseeing requests for material master creation, changes and maintenance with respect to companywide processes and procedures for Commercial, Clinical and Raw Material Basic and Quality Master Data for GPLM, Oracle E Business Suite (EBS) and Kinaxis Rapid Response.
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Licensed Clinical Social Worker (LCSW), Licensed Marriage and Family Therapist (LMFT), or Licensed Professional Clinical Counselor (LPCC) in the state of California. This position involves a combination of clinical supervision, program management, and community engagement activities.
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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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Experience with developing study concepts for clinical development and clinical trial designs with cross functional input, including biostatistics, observational research and patient reported outcomes in Phase 1, 2 and/or 3 clinical trials in obesity or diabetes.
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The selected candidate will perform duties encompassing all aspects of insurance defense, including initial investigation and legal analysis and advice, preparing and filing legal pleadings and documents, performing legal research, preparing for and conducting pre-trial discovery, preparing for and aggressively handling hearings and trials, and conducting post-trial activities where appropriate.
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Interpret and communicate clinical trial data. Five (5) or more years of clinical research experience in the biopharmaceutical industry (biotech, pharmaceutical or CRO company) in obesity or obesity-related conditions.
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Performs other cross training tasks, as assigned, including, but not limited to the following areas; Studio Operator, Master Control operator and, Playback, TOC Operator. Performs other cross training tasks, as assigned, including, but not limited to the following areas; Studio Operator, Master Control operator and, Playback, TOC Operator.
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An ideal candidate will meet the Secretary of the Interior's Professional Qualifications Standards for Architectural Historian; however, in lieu of a Master of Arts, candidate may hold a Bachelor of Arts in History or a closely related field.
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California Clinical Genetic Molecular Biologist Scientist License upon hire, Or. California Clinical Laboratory Scientist Biochemistry Special License upon hire. California Clinical Laboratory Scientist License California upon hire, Or.
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Serve as a Principal Investigator for clinical trials, Phases I to IV, where you will be responsible for the clinical research conduct and quality assurance, as well as supervising sub-investigators in their clinical trial work.
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Experience with Healthcare data, e.g., clinical trial data, electronic medical records, and insurance claims; or Bioscience's data, e.g., protein or small molecule data, or bioinformatics; or Biopharmaceutical manufacturing.
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Candidates must have a Master of Social Work degree from a Council on Social Work Education (CSWE) accredited program AND a doctorate degree in Social Work, Social Welfare, or a related field. Assistant Professor - Master of Social Work Program #24-20.
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clinical trials trial master jobs Title: trial master in Culver City, CA
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