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As lead of the Study Core Team the CS will lead via a matrix organization Epidemiology, Biostats, Clinical Operations, Medical/Scientific Affairs, Regional, Pfizer laboratory assay group, and external team members.
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The Scientific Research Manager will report to the Department Chair and works with the Business Office of the Department of Pathology using their field-specific knowledge to develop and advance new strategic directions for the department, namely developing infrastructure and workflows to support diagnostic innovations at the Institute as well as developing scientific and educational programs with our partnering clinical departments.
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The Medical Science Liaison (MSL) is a field-based scientific expert that executes Pacira’s medical affairs strategy. The primary role of the MSL is to conduct scientific exchange with Health Care Providers (HCPs), communicate clinical and business insights to Pacira, and support evidence generation initiatives in the assigned therapeutic area(s) within a specified territory.
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This includes collaborating with Clinical Research, Clinical Operations, Medical Scientific Affairs, and/or vendors to develop and monitor the clinical trial safety.
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Research is supported by the National Heart, Lung, and Blood Institute, American Society of Nephrology and the BWH Khoury Innovation Fund. Under the supervision of the Principal Investigator and research staff, the Research Analyst Intern will conduct analyses with and develop pipelines for various types of omic data as well as clinical datasets from epidemiologic studies and clinical trials.
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You will have deep technical knowledge, a strategic mindset, and clear, forwarding-thinking leadership in preclinical models of human disease, establishing PK/PD relationships for gene therapy technologies, and a proven track record of successfully leading research programs from discovery into early clinical testing.
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Contribute as a key member of the project teams that provides strategic, technical and scientific leadership for progression of program from discovery research through development and contribute as a subject-matter expert for clinical development and overall asset strategies.
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The Scientist, Neuromuscular Research role is an exciting opportunity to contribute to the expansion of Dyne’s research pipeline, building on the positive clinical data in DMD and DM1 programs.
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As part of the DSRE, Pathology team, you will report to the Senior Director DSRE - Pathology and serve as a project pathologist and/or project toxicology representative to project teams within the Global Pathology group in Drug Safety Research and Evaluation (DSRE) through the provision of anatomic/clinical pathology and toxicology expertise.
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JOB SUMMARYThe Research RN, NCHRI works directly with the physician in accurately and professionally executing all clinical research projects in an acute care/inpatient setting (ED, Cath Lab, ICU, EP lab, Step down and OR) as well as the ambulatory and ancillary areas.
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Collaborate closely with other groups within the early CVRM therapeutic area to provide experienced clinical insight into pre-clinical scientific activities such as target selection, lead generation and optimization, clinical pharmacology and in vivo/in vitro studies.
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Join Takeda as a Scientific Director, Pathology in Cambridge, MA, where you will be responsible for active cross-functional collaboration, interdisciplinary project team participation, scientific leadership in the design and implementation of safety assessment strategies to support program advancement and decision-making, primary evaluation and peer review of pathology specimens and data, preparation and review of regulatory documentation, study reports and manuscripts.
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The Clinical Research Associate/Clinical Research Coordinator I (CRA/CRC I) works under general supervision to enroll eligible patients to clinical research protocols and manage all aspects of data collection and submission for multiple cancer studies.
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Our world class scientific founders include Professor David Liu (HHMI, Broad and Harvard) and Professor Keith Joung (Arena BioWorks, formerly MGH), and we are funded with a significant capital investment by leading life science venture capital firms including Newpath Partners, Atlas Venture, F-Prime Capital, and 5AM Ventures.
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The primary role of the Director, Regulatory Affairs - CMC is to create and/or manage contributions from others for CMC regulatory submission documents. This position reports directly to the Senior Director, Head of Regulatory Affairs - CMC. The Director, Regulatory Affairs - CMC will be responsible and accountable for CMC submission documents while successfully up-holding the vision for the function and help mentoring junior team members.
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clinical research scientific affairs jobs Title: director Company: Regeneron Pharmaceuticals Inc in Boston, MA
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