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Electrocardiogram (ECG), venipuncture, immunizations, setting up procedure trays, specimen collection and/or Clinical Laboratory Improvement Amendments (CLIA) waived testing as directed by Provider.
Full-timeExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Minimum 3 years of clinical research, public health research experience or research working with high-risk patient populations. Previous experience with grant writing, IRB submissions, data management, and database development, preferred.
ExpandApply NowActive JobUpdated 28 days ago - UpvoteDownvoteShare Job
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ICON plc is a world-leading healthcare intelligence and clinical research organization. Demonstrates technical expertise and background in the use of medical writing templates and software (eg, Please Review, Documentum-based platforms, etc.
Full-timeExpandApply NowActive JobUpdated 26 days ago - UpvoteDownvoteShare Job
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Development formulation from preclinical to clinical phase in accordance to FDA and EMEA guidance. Radio metal chemistry, radio-formulation development analytical expertise, CMC writing and the ability to integrate learnings and failures from others are some things the lead must have.
Full-timeExpandApply NowActive JobUpdated 14 days ago - UpvoteDownvoteShare Job
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Responsibilities: Demonstrate ability to diagnose and treat children/youth and families Provide individual and group therapy, including structured and process groups, within a variety of settings, based on group/client needs and Clinician credentials Depending on level of experience, provide clinical consultation and training to staff Act as the primary contact for the service plan with the ability to expertly and succinctly communicate at all levels both verbally and in writing.
ExpandApply NowActive JobUpdated 19 days ago - UpvoteDownvoteShare Job
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The Laboratory Supervisor is responsible for managing assigned selected aspects of laboratory processes or shifts, which may include workflow, quality control process, writing/reviewing procedures, performance improvement activities, training of new employees, advanced problem solving for customers and coworkers, department equipment or computer maintenance and upgrades, or other tasks assigned.
Full-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Understanding of Clinical Note writing in DAP format. is responsible for performing Patient care activities in our new state of the art facility as directed by the attending physician, Medical Director and Clinical Director.
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Demonstrated ability to produce clear, high-quality writing in the English language AND demonstrated experience in the preparation of a broad range of complex clinical and regulatory documents and global submissions.
$218,978 - $274,868 a yearFull-timeExpandApply NowActive JobUpdated 28 days ago - UpvoteDownvoteShare Job
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Academic tests (listening, writing, and speaking) offered by the International English Language Testing System (IELTS). Possession of a permanent, full, and unrestricted license to practice veterinary medicine in a State, District of Columbia, the Commonwealth of Puerto Rico, or a territory of the United States that includes successful completion of the North American Veterinary Licensing Examination (NAVLE) or its predecessors, the National Board Examination (NBE) and the Clinical Competency Test (CCT.
Full-timeExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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We serve our customers through a globally integrated network of facilities in North America, Europe, and Asia. This enables us to offer a comprehensive range of services including drug discovery solutions, process & pharmaceutical development services, clinical trial supplies, commercial supply of APIs, and finished dosage forms.
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Current Drug Enforcement Agency (DEA) and Department of Public Safety (DPS) registration (if applicable to state), for prescription writing. Escalate acute clinical care concerns appropriately, involving Medical Director, Clinic Manager and APRN, per Walmart Health policy.
Full-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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This position requires both classroom management and management of instructional responsibilities to include, but not limited to, implementing CARE principles, delivering assessment tools, creating lesson plans, writing IEPs, coordinating with the clinical team, supervising educational technicians, involvement in TCI safety restraints, BHP, ISP, and IEP tracking and various other duties in a day treatment special education setting.
Full-timeExpandApply NowActive JobUpdated 12 days ago - UpvoteDownvoteShare Job
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Oversee the full life cycle of multicenter randomized clinical trials including study design and implementation; data collection tool development; data quality assessment and ongoing monitoring; regulatory reporting; statistical analysis; interpretation of results and manuscript writing for the Peripheral Artery Disease (PAD) research group.
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Responsible for the oversight of clinical study execution in close collaboration with Clinical Operations lead, internal and external stakeholders (data management, biostatistics, programming, drug safety and PV, medical imaging, medical writing, research, and discovery.
Full-timeRemoteExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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This team is seeking someone to draft, edit and manage documents for pre-clinical, IND-enabling studies that are being led as we continue to develop and move products through our scientific pipeline.
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