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Our research aims to improve quality of life, well-being, symptom and pain management, and reduce caregiver burden:For example, a Clinical Research Coordinator to support a large multi-site clinical trial study that focuses on the comparison of care delivery models to support older adults with complex healthcare needs.
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Bachelor’s degree required in a field relevant to clinical research, and 5 plus years experience with project management and experience working on clinical trials (multi-center, oncology trials preferred.
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The company has approved medicines that treat the underlying causes of multiple chronic, life-shortening genetic diseases — cystic fibrosis, sickle cell disease and transfusion-dependent beta thalassemia — and continues to advance clinical and research programs in these diseases.
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Provide timely reports to HilleVax management on Research Compliance metrics and state of GCP compliance of HilleVax-sponsored clinical trials. Provide GCP quality support to clinical research functional areas (e.g., Clinical Development, Clinical Operations, Medical Writing, Medical Monitoring, Data Management, Biostatistics & Programming, Regulatory Affairs, Clinical Supplies Management, Pharmacovigilance.
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Working familiarity with analysis of research data, biostatistics, pharmacology and pharmacokinetics, international standards for Good Clinical Practice (GCP), clinical study design, ethics committee/Institutional Review Board review, preparation of manuscripts, abstract/posters, and oral presentations, overall drug/device clinical development.
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The Clinical Trials Monitor (CTM) monitors and audits the investigator-initiated clinical research studies across all disease groups in the Cancer Clinical Trials Office. The position is primarily remote but may require some on site work.
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Minimum 3 years of clinical research/drug development experience in biotech, pharmaceutical, or contract research organization (oncology experience a plus). Synterex offers remote or on-site services, with a focus on providing clear, concise, accurate, and fully compliant documentation, from early drug development through post-approval.
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BA/BS degree required with a minimum of 2 years relevant clinical research experience working at an Investigator Site, Sponsor or Clinical Research Organization. The CTA position is focused on providing support associated with the planning, start-up, maintenance, and closeout of clinical trials.
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The CICL provides echocardiography core laboratory services for primarily large-scale global clinical trials responsible for site training and interface as well as echo analysis of images received.
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You will support the clinical team with the implementation and oversight of clinical trials, focusing on the areas of clinical operational strategy, trial logistics planning, enrollment, site monitoring, data quality, and study reporting.
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Must have: 3 years of CRA monitoring experienceExperience with Monitoring IVD studiesLab testing/instrumentation experienceIdeally experience working on Point of Care Waived CLIA studiesJob DescriptionResponsible for the management and monitoring of clinical study sites and reference laboratories to support clinical development programs.
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Providing support for Innovative clinical trials program development Create SOPs, training documents, educational tools and templates to educate research staff on data management resources and platforms Organize PETAL DMC internal documentation and file storage to optimize efficiency 2.
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Our seamless in-office and 24/7 virtual care services, on-site labs, and programs for preventive care, chronic care management, common illnesses and mental health concerns have been delighting people for the past fifteen years.
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For example, a Clinical Research Coordinator to support a large multi-site clinical trial study that focuses on the comparison of care delivery models to support older adults with complex healthcare needs.
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The Clinical Research Associate will manage the daily aspects of investigational site activities on a global pivotal trial. Clinical research certification (ACRP or SOCRA, Clinical Coordinator / CRA certification) preferred.
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on site clinical research jobs in Boston, Holdrege, Nebraska
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