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The Senior Director, Dana-Farber Cancer Institute (DFCI’s) Clinical Research Network (CRN) oversees clinical research administration functions occurring outside of Boston’s Longwood Medical Center Area – including clinical trials activities and teams across DFCI’s Collaborative, External, and Regional Sites.
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Analyze data from clinical trials, real-world evidence, and other sources to support the value proposition. Expertise in designing and executing studies to generate clinical and economic evidence, including data analysis from clinical trials and real-world evidence.
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Job Summary: Under the administrative direction of the Nurse Director, the Clinical Nurse Manager identifies, develops, and oversees policies and procedures that support excellence in clinical practice and fosters an environment of care which reflects the mission and vision of Newton-Wellesley Hospital.
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The Senior Manager/Associate Director, Supply Chain Planning will be responsible for supply chain planning for clinical supplies (clinical trial material) across a number of small molecule drug development programs in support of Xenon’s clinical trials.
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We are seeking applicants with demonstrated experience providing culturally competent behavioral health care to a diverse adult population including LGBTQ individuals, people of color, individuals with substance use issues, survivors of abuse, survivors of community violence, medically complex and vulnerable individuals, young adults, and older adults.
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The Director of R&D Quality, GCP - Cell Gene Therapy (CGT) reports directly to the Head of RDQA and is a trusted advisor and partner to clinical and quality stakeholders and business partners. This role supports the program and study level quality leads in key quality related clinical activities and deliverables for all CGT programs across the Vertex clinical portfolio.
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Since its founding in 2000, the firm has originated and fostered over 100 scientific ventures, generating more than $34 billion in aggregate value and conducting over 50 clinical trials for novel therapeutic agents.
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In addition to its wholly owned clinical assets, Dragonfly has a deep pipeline of wholly owned preclinical candidates discovered using its proprietary platform, as well as productive collaborations with Merck, AbbVie, Gilead and Bristol Myers Squibb in a broad range of disease areas.
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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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Advanced degree in a relevant discipline (e.g., analytical chemistry, biochemistry or related field) and 6-8+ years of analytical development & quality control experience with complex biologics, particularly Fc-fusion proteins and monoclonal antibodies from early to late-stage development (or equivalent combination of education and experience.
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The role represents the CPQP function on drug development teams, leads CPQP sub-teams, and owns strategy and delivery on posology for early and late-stage clinical trials while collaborating with clinicians, clinical operations, bioanalytical, biomarker, pharmacovigilance, regulatory and CMC groups.
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Experience in managing data management tasks for Phase III clinical trials. 8-10 years of clinical data management experience, previous work with CROs and Data Management vendors is required, working in a global/cross cultural setting is preferred.
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Exciting opportunity to join our EP Lab that is internationally recognized for its innovative advances in clinical electrophysiology, cardiac arrhythmias and pacemakers. We’re helping patients get the best care possible by working on digital health experience, analyzing big data to streamline the delivery of care, and reaching out to medically complex patients to better understand their needs.
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Actively participate in Regional and National calls and stay abreast of key topics in order to effectively cascade communications within the Complex. Manage risk and assure positive audit results throughout the Complex in partnership with Risk and Compliance.
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Melrose/Wakefield Hospital and Lawrence Memorial Hospital are distinguished by the range of high-quality clinical care and services. Educates and in-services staff on clinical skills, acts as a clinical liaison to other staff.
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complex clinical trials work jobs Company: Emory University in Brookline, MA
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