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The Clinical Therapist, EPS provides clinically competent assessment to determine appropriate level of care in the least restrictive environment which may include psychiatric assessment, safety planning and collaboration with members of the Behavioral Health clinical team to determine case disposition in an accurate and timely procedure within program policies and procedures.
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Ensure the timely and efficient delivery of all biomarker operational aspects across vaccine clinical trials: accountable for planning, coordinating, and overseeing all operational activities required to manage the flow of biomarker samples from planning, collection, analysis, data delivery and final sample disposition with support from the Biosample Operations Manager.
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Hire and provide oversight of Quality personnel with expertise in Good Clinical Practice (GCP), Good Pharmacovigilance Practice (GVP), Good Laboratory Practice (GLP), and Good Manufacturing Practice (GMP.
$200,000 - $250,000 a yearFull-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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EXPERIENCE For Connecticut, consistent with LCSW licensure requirements, 3,000 hours of post-masters social work experience and 100 hours of post-masters clinical supervision. As the clinical expert, the scope of practice includes, but is not limited to, diagnostic assessment, counseling, psychotherapy, brief treatment, crisis intervention, mental health consultation, teaching/mentoring, and/or other project/task force participation as assigned by supervisor.
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Employ decision support tools, clinical judgement, and available evidence to expedite a nursing diagnosis and disposition in a complete and organized manner, realizing limitations and seeking assistance as necessary.
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Duties will include, but are not limited to budget development for physician practices in partnership with finance manager, physician compensation support, capital equipment procurement and disposition, space utilization in the clinical space, and staff supervision.
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Answers the telephone crisis line and obtains all pertinent demographic, clinical, marketing and third party information to determine the appropriateness of face-to-face telephonic assessment and clinical disposition of the caller; seeks supervision when caller requests information/data unfamiliar to counselor.
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Maintain excellent working relationships and communication with the Other physician members of the hospitalist practice, members of the medical, nursing and clinical staff and hospital leadership.
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Following a 2022 merger of CNSI and Kepro, Acentra Health combines clinical services, technology solutions, and data analytics to accelerate better health outcomes. Maintain detailed logs and document the disposition of incoming and outgoing calls, ensuring accurate record-keeping.
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Coding Quality Specialist will work collaboratively with various CHRISTUS Health Departments, including but not limited to the Regional Coding Managers, HIM, Compliance, and Clinical Documentation Specialist to ensure feedback is shared and reported for education and training purposes.
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Maintain regular communication with the Director of Business Development, Director of Clinical Operations and Patient Care Manager in order to follow-up for every admission. Ability to maintain a positive, stable disposition in performing, working in association with staff, patients and families.
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A minimum of 3 years’ experience in a GMP manufacturing environment with a bachelor’s degree in Biology, Chemistry, Chemical engineering, Biomechanical engineering, Bioengineering, Biomedical engineering, Biochemistry or related field or seven years of experience in a clinical quality assurance environment.
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Make quality control decisions regarding the disposition of an assay or test. Minimum one (1) year full-time experience or training(high complexity testing)in a clinical laboratory settingfor those with BS/BA in Chemistry or Biology.
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Partner with other disciplines of integrated drug discovery and development, especially pharmacokinetics and drug disposition, Drug Safety, Regulatory, and Translational Sciences, to develop translational preclinical packages for gene therapy clinical candidates.
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E COAs, analytical validations/transfers, process validations, master & executed batch records, label proofs, specifications, executed batch record review and batch disposition of Drug Substance, Drug Product and Finished Products (oral solid dosage forms, parenteral, radio labeled materials.
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