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Kiel Laboratories is looking for an analytical Project Manager that understands the early clinical drug development process and pharmaceutical terminology. Good business judgment and a strong understanding of the unique aspects of the drug development process.
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Responsible for the overall administration, clinical planning, development and operations of the rehab program. Current state license as an Occupational Therapist / OT, Physical Therapist / PT, Speech Language Pathologist / SLP, Occupational Therapy Assistant / COTA or Physical Therapy Assistant / PTA or proactively in the process of the application process for current state licensure as an OT, PT, SLP, COTA or PTA. Current CPR certification.
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We structure ourselves to deliver scientific expertise to our clients; collaborating closely with them to support the development of medicinal products through the drug development process and onto market.
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The Process Engineering Manager is a licensed professional Lean Six Sigma Black Belt who possesses a strong understanding of Lean Six Sigma process design and improvement methodologies that can be utilized to optimize and transform clinical workflows in the acute care setting.
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The Registered Nurse (RN) provides clinical supervision for entry level nurses and assists in their development. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process, please contact us at (844) 257-6925.
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Complete nutritional assessments of patients and documents results using the Nutrition Care Process and the Nutrition Focused Physical Exam. Calculate patients nutritional needs based on accepted Standards of Care. Make daily decisions independently but obtain input from RDII, RDIII, Lead Registered Dietitian or Clinical Nutrition Manager for complicated cases or issues.
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Reporting to a lead within the Process Sciences team, CARGO Therapeutics is seeking a highly motivated and versatile individual to join us as a Senior Scientist in Analytical Development within the Process Sciences organization.
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Over the past few years, we have been able to significantly expedite the drug development process, evidenced by our acceleration of over 300 clinical trials and reducing trial durations by up to 50.
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Responsible for coordination of orientation of all nursing personnel; representation of CHRISTUS in community activities; and planning, development, implementation, and evaluation of nursing continuing education programs.
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It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations.
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2) Knowledge and experience in capital project lifecycle management including conceptual design, scope, resource estimate & cost estimate development, business case development, detailed design, engineering, commissioning, validation, and project execution, as it relates to Plant Automation and process control systems with GMP biopharmaceutical production facility equipment/systems in support of Drug Substance, Drug Product and Supply chain plant operations.
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Clinical judgment and decision makingUtilizes the nursing process and a critical thinking approach to provide patient care that incorporates the mind, body and spirit; is individualized, goal directed, and consistent with current standards of safety.
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De-Escalation Certification (required if Educator in ED or BHU Units). BLS/ACLS/PALS Instructor Certification. RN license in state of employment or a compact state. We endeavor to make this site accessible to any and all users.
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Prepare and analyze clinical data for research purposes, process improvement, utilization management, mandatory reporting, and more. · Provide staff management to including hiring, development, training, performance management and communication to ensure effective and efficient department operation.
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Lead the ReCAP process (review of all Medical Affairs sponsored clinical trials and Investigator Initiated Sponsored studies) for applicable products. The GMAL, will be a member of the Compound Development Teams (CDTs), the Safety Management Teams (SMTs) and Global Commercial Teams (GCTs), as well as an ad hoc member of the Clinical Team and Global Market Access Team, and will be responsible for development of the Global Medical Affairs plan that reflects prioritized regional needs and are included in the overall compound development plan.
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