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Are you a Licensed Clinical Alcohol and Drug Counselor (LCADC) in New Jersey in South Dakota looking to launch a private practice, or grow your existing practice? Licensure: You’re a fully licensed, Licensed Clinical Alcohol and Drug Counselor (LCADC) in New Jersey.
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Leads planning and management of the assigned clinical study(ies) from feasibility through closeout activities for region, in line with global study timelines. 4 or more years of progressive experience in clinical research within biotech, pharma or CRO industry.
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Experience with clinical trial databases (e.g., Medidata Rave, Veeva, etc. As a CTM, you will be responsible for planning and managing our early development clinical trials in kidney disease while ensuring high quality data and timely clinical trial conduct per GCP standards.
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Current California State Clinical Laboratory Scientist License to include the limited CLS license. Clinical Laboratory Scientist. Analyzes clinical laboratory specimens following the standard methods and procedures approved by the Laboratory Director or designee.
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Reporting into the Director, Clinical Operations the Clinical Project Associate will support the in-house day-to-day operational activities for the successful execution of a trial(s). Title: Clinical Project Associate.
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DescriptionThe Senior Clinical Data Manager (CDM) is responsible for data management activities across one or more studies from study start-up through study closure to ensure completion per established project team goals and objectives.
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Capable of independently authoring and delivering ADME and Clinical Pharmacology sections of regulatory submissions. The Senior Director of Clinical Pharmacology will develop clinical pharmacology plans and deliver data packages to help advance the clinical development of a diverse pipeline of therapeutic modalities (e.g., small molecules, biologics, nucleic acid therapeutics, and gene therapies.
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Author clinical pharmacology sections of NDA and/or BLA filings, clinical study reports, protocols, investigator brochures, regulatory responses, and other submissions. Represent Clinical Pharmacology on project teams and cross-functional initiatives and in global health authority meetings.
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Knowledgeable in CRF design, interactive response technology (IRT) systems, and clinical supply logistics. Manages Clinical Operations study start up trial activities for one clinical trial.
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Reporting to the Director of Clinical Services at St. Anthony Medical Clinic (SAMC), the CPM will manage the companion program with a comprehensive therapeutic approach and professional behavioral guidance.
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Essential Duties and ResponsibilitiesPerforms full range of Clinical Laboratory tests available at Chinese Hospital CLIA Laboratory, particularly in Hematology, Chemistry, Immunoserology, Blood Bank, Clinical Microscopy and Microbiology.
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TITLE: CLINICAL COUNSELOR (AMFT, ASW, or APCC ) Supervision Provided. The Clinical Counselor will also develop and maintain effective relationships with personnel from the CBHS System of Care service providers, as well as related services such as the SFGH Department of Psychiatry, SF Police Dept., the SF Fire Department, Emergency Medical Transport Services, and providers of basic supports such as housing, temporary shelter, and entitlement advocacy.
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As a Clinical Data Manager/Analyst in the Quantitative Sciences organization, you will be responsible for supporting and managing the collection, capture, quality, and integrity of data, from diverse sources, including electronic health records, eCRF, ePRO, digital health technologies including apps and sensors, digital biomarkers, advanced specialty labs, images, and others.
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IDEAYA Biosciences (NASDAQ: IDYA) is a public, clinical-stage precision medicine oncology company committed to the discovery and development of targeted therapeutics for patient populations selected using DNA sequencing and other molecular diagnostics.
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Understanding of the related disciplines (i.e. biostatistics, regulatory, pharmacology and toxicology research, cell therapy manufacturing, clinical pharmacology and pharmaceutical sciences) Reporting to the Head of Clinical Development, this individual will have oversight of and accountability for clinical trials from study start-up to BLA approval.
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Title: clinical Company: F Hoffmann La Roche in South San Francisco, CA
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