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In the Clinical Research Center (CRC), the Administrative Coordinator is responsible for providing administrative support to the Senior Investigator of Clinical, Behavioral & Outcomes Research, the CRC Nurse Manager and Manager of Administrative Services.
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The Clinical Finance Office seeks a Dental Financial Coordinator to oversee the workflow of dental clinical finances related to state Medicaid/Medicare programs, including MassHealth and other identified programs administered by Dentaquest and Skygen/Scion.
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Summary The Senior Clinical Compliance Auditor is responsible for developing, auditing plans, and collaborating with Operations and Revenue Cycle in auditing/monitoring compliance requirements across all Company business units and service lines.
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Research studies are investigator initiated and industry sponsored and range from observational studies and registries to biobanking to interventional clinical trials of novel treatments.
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You will manage clinical trials from start-up through close-out to ensure both internal and external deliverables are on time and on budget while facilitating collaboration across functional areas.
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Can proficiently perform all duties of an LTA. Performs other clinical laboratory assistant duties and responsibilities as required at the direction of lab support supervisor. Qualifications Minimum Education/Experience: High School Diploma or EquivalentGraduate of Phlebotomy Training program preferred.
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The Associate Director/Senior Manager of Clinical Quality will develop, manage, and improve existing quality systems to ensure appropriate controls for EyePoint in-house GCP and GLP capabilities.
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May assist in management of additional clinical technologies, as assigned, that are leveraged in clinical trials, developing system vendor strategy, partner selection, system standards and internal processes to ensure compliant systems development and operations.
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The Manager will oversee GCP activities across various areas of development, ensuring compliance, and quality execution of clinical trials. Fundamental knowledge of US, EU, and international regulatory standards and guidelines for clinical trials.
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Assess both scientific and development feasibility, evaluating strategic fit with portfolio, evaluating complete or ongoing clinical trials, assessing regulatory interactions and future development plans, interacting with upper management of potential partner/acquisition companies during due diligence visits and alliance negotiations, and participating on internal assessment teams together with commercial colleagues.
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Experience in Good Clinical Practice (GCP) and regulatory compliance guidelines for clinical trials. In this exciting role as the Senior Field Clinical Research Specialist, you will be responsible for clinical trial site management, case coverage, and clinical trial data tracking.
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Solid working knowledge of Pharmacokinetics, PK/PD principles applied to modeling, ADME and clinical pharmacology concept and understanding of regulatory guidelines on DMPK/ clinical pharmacology studies to support early oncology drug development.
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Uses management skills to ensure disease groups have appropriate internal organization to effectively comply with regulatory requirements for clinical trials. Day (United States of America)The Clinical Trials Specialist II is responsible for fostering and enhancing inter-team and inter-group collaboration, serving as a source of knowledge and expertise that can be used as a resource by more junior staff.
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The Clinical Trial Manager is responsible for the management of clinical studies across phases including actively participating in a variety of activities to support and facilitate the efficient conduct of patient trials in our clinical research programs.
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Serve as part of the multidisciplinary review team to complete utilization review of client records and implement corrective actions for all clinical documentation in order to maintain agency compliance with state regulations and mental health professional standards.
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Title: clinical trials Company: Parexel in Newton, MA
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