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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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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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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 a Trial Attorney, you’ll represent clients under both commercial and personal lines insurance policies as lead counsel, with moderate to low guidance and oversight, and also may handle cases as part of a larger team as needed.
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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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Knowledge of clinical research budgeting and the clinical trial life cycle: study start-up through study closure. The Medicare Coverage Analyst (MCA) is responsible for reviewing clinical research protocols, Informed Consent Forms, Clinical Trial Agreements, and other relevant study-related documents to create a coverage analysis/billing guide.
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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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AMDA offers various pathways for students to receive unparalleled performing arts education taught by world-class industry professionals, including Professional Conservatory Certificates as well as undergraduate and graduate degrees (Bachelor of Fine Arts, Bachelor of Arts, Associate of Occupational Studies, Master of Fine Arts and Master of Arts.
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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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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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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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Handle all facets of litigation, including:Motion practice Discovery Alternative dispute resolution Trial preparation. Manage breach of contract and bad faith claims from inception to trial.
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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 Los Angeles, CA
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