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Provides ad-hoc programming support to Clinical Operations, Data Management, Statistical Programming, Biostatistics, Drug Safety, Clinical Science, Medical Writing and Drug Safety to ensure rapid access to clinical study data for data cleaning/validation, SAS listings review, TLF, dry runs, etc.
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Working independently, under the general supervision of senior personnel, the Research Associate will perform highly specialized experimental procedures involving in vitro protocols, advanced molecular genetics, and cellular biology techniques.
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The Research Associate will be responsible for developing LNP formulations and processes to support company's in vitro and in vivo pre-clinical studies. Perform experiments that involve preparation and physiochemical characterization of nanoparticles.
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This role requires combining a high level of competency and experience in Strategic Sourcing with solid understanding of science and the drug discovery and development process and the business that supports it.
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This is a unique opportunity to be part of a thriving clinical-stage biotech company bringing innovative technology to the global market. Vaxess, a venture-backed clinical-stage life sciences company, is building a team of exceptional people to rapidly advance products on the MIMIX™ platform.
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Research and Development is at the heart of fulfilling Pfizer's purpose as we work to translate advanced science and technologies into the therapies and vaccines that matter most. Whether you are in the discovery sciences, ensuring drug safety and efficacy or supporting clinical trials, you will apply cutting edge design and process development capabilities to accelerate and bring the best in class medicines to patients around the world.
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EyePoint is seeking an experienced Program Manager, reporting to the SVP, Program Leadership, who will work collaboratively on the assigned projects and strategic initiatives to manage and integrate diverse drug development activities spanning all phases of clinical development.
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The journal’s scope spans the full breadth of cancer science and medicine, ranging across biochemical/molecular studies, tumor biology, systems biology, clinical-stage research, and population science.
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In addition, the Department of Surgery will be engaged in the newly announced and exciting clinical collaboration between Dana-Farber Cancer Institute, BIDMC, and Harvard Medical Faculty Physicians (HMFP) to establish New England’s only free-standing adult inpatient cancer hospital.
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The Associate Director, Biostatistics is responsible for statistical activities in support of clinical trials, including contributing to trial designs, authoring statistical sections of protocols, preparing statistical analysis plans, and reviewing and interpreting the analysis of clinical trial data.
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The Associate Director will be accountable to the GRL and Global Regulatory Science Precision Medicine Head for development of appropriate regional Precision Medicine and Digital Health regulatory strategy(s) and their timely delivery.
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AN IDEAL CANDIDATE WOULD HAVE: Must have a valid Registered Nurse's license from the Commonwealth of Massachusetts Must have a Bachelor's degree in Nursing or an Associates of Science Degree in Nursing and at least one (1) year of clinical experience and/or nursing in a community or long term care setting; or an Associate Degree in Nursing and five years of experience, with two years of community based nursing or long term care setting.
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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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Candidates must have at minimum a Bachelors degree in a health or science related field, minimum one year of clinical research experience or relevant direct industry experience (e.g., CRC), ability to travel nationwide, must be detail-oriented, strong time management, and communication skills.
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We are looking for an Associate Director in Clinical Pharmacology who will be a key member of our multidisciplinary drug development teams. Collaborate cross-functionally with other departments, including Clinical, Regulatory, Translational Science, Biometrics, Clinical Operation and Pharmacovigilance.
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