72 web-programmer-developer-"https:" "https:" "https:" "https:" "https:" "https:" "https:" "UCL" "UCL" Fellowship positions at Northeastern University
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Number: 6791178 BridgeBio Pharma, Inc. Regulatory Affairs Postdoctoral Research Fellow About the Opportunity About the Opportunity Northeastern University Pharmaceutical Industry Fellowships Program is a
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Inflammation, Neuroscience, and Rare Genetics & Hematology. The two-year Takeda Global Medical Affairs Fellowship Program is designed to prepare post-doctoral scholars for rewarding careers in
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Number: 6791168 Takeda-Global Regulatory Affairs Postdoctoral Research Fellow About the Opportunity About the Opportunity Northeastern University Pharmaceutical Industry Fellowships Program is a two-year
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Discovery) in the Department of Pharmaceutical Sciences, Bouve College of Health Sciences, Northeastern University, Boston. Thakur Lab has been at the forefront in developing GPCR (cannabinoid receptors 1 and
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Researcher will be based out of either the Boston, MA or Portland, ME campus and conduct applied research, prepare work for submission to journal/conference publications, contribute to extramural funding
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the medical plan, strategic publication plan, and disease state communication framework Collaborate with US and Global cross-functional stakeholders to prepare materials for key scientific conferences and
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Northeastern University faculty in professional and career development, teaching, service, and scholarly activities. PharmD Fellowship Program - Global Scientific Communications Location: Scholar Rock, Cambridge
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discovers, develops, and delivers life-changing therapies for people with serious diseases that have high unmet need. Scholar Rock’s Global Scientific Communications Fellowship is a two-year program that
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. Early Assets Medical Affairs partners with experts across the organization to guide each unique investigational program as it enters the clinic and throughout its Ph 1 and Ph 2 development. Working cross
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regulatory milestones Participate in cross-functional meetings to support and contribute to the clinical development plan and regulatory strategy Conduct guidance and precedent research to support regulatory