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Position Title: Clinical Data Scientist. Ability to develop, evaluate, and implement workflows for technology, optimize and standardized existing techniques and workflows with respect to experimental HT mRNA generation process workflow including DNA & IVT-RNA production, and in vitro/in vivo screening is desired.
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Specialized Clinical Educator will support clinical staff in the implementation of curriculum instruction and in maintaining a safe and nurturing environment. Report any client incidents/concerns to Program Director, Clinical Director and/or the Milieu Manager.
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Working Title : Clinical Lab Scientist II, Laboratory Immunology - Day. The Clinical Laboratory Scientist II (CLS II) functions with general directions from senior technical personnel. Valid California Clinical Laboratory Scientist license or limited license appropriate for the area of responsibility.
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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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Proven track record of leading biomarker programs from conception through validation and implementation in clinical trials. As a Senior/Principal Scientist in Clinical Biomarkers, you will be a key player in their research efforts to develop therapies that combat neuromuscular disease.
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The Clinical Research Coordinator, Level 1 (CRC1) is a research professional who ensures oversight and compliance of both system-wide and local SHC clinical research activities. Reporting to the Hospital Administrator and to the Research Programs Office at SHC International Headquarters, the CRC1 provides support in accordance with SHC’s policies and procedures, SHC’s hospital regulations, the Code of Federal Regulation, and Good Clinical Practice.
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Offers strategic leadership, expert guidance, and thorough oversight to ensure the seamless management of all clinical trials. Based in their Boston office, you will be responsible for driving the successful execution of clinical trials from early-phase trials through phase III. The Director will guide the planning and management of these programs, making sure everything runs smoothly.
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You will be responsible for establishing and leading a world-class clinical operations function to conduct industry-leading gene therapy clinical trials across Ensoma's portfolio.
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Utilizes advanced knowledge of clinical trials to serve as subject matter expert regarding protocols, regulatory compliance and sponsor relations. Performs activities to support the operational needs to clinical trials to include collecting and shipping of protocol-related lab samples and devices, ensuring investigational devices are ordered, received and securely tracked and ensuring protocol required imaging is done in accordance with protocol requirements and sent to the appropriate core labs in the specified format.
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Plan and conduct clinical trials. Demonstrated track record in leading cross-functional teams and work streams (pharmacovigilance, biostatistics, clinical operations, and regulatory affairs.
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Associate Director of Data Science specializes in the development of novel digital endpoints in late stage clinical trials using data science, statistical learning, and innovative machine learning methods on multi-modal datasets including clinical data, real world evidence, imaging, wearables, and other biomedical data sources.
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If applicable to set up regular meeting with MSL (Medical Science Liaison) at LMA (Local Medical Affairs) who can support Clinical Operations at various steps (site qualification, site recruitment.
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The Director Trial Master File (TMF) and Clinical Documentation spearheads the vision and strategy for records management of clinical trial documents. Foster effective relationships with stakeholder functions to achieve TMF objectives and serve as a subject matter expert on TMF across all functions involved in clinical trial execution.
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Direct experience with different Data Management systems and technologies, Clinical Data Management Systems and CDISC data standards. Deep understanding of drug development, study conduct processes, GCP and regulations related clinical data management as well as ICH guidelines, FDA/EU regulations.
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Reviews clinical trial and non-human primate data ensuring integrity, privacy, consistency and compliance for multiple trials at a time. The Clinical Trials Monitor (CTM) monitors and audits the investigator-initiated clinical research studies across all disease groups in the Cancer Clinical Trials Office.
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Title: clinical trials Company: Parexel in Newton, MA
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