Clinical Development Jobs in Cambridge
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Search Results - Clinical Development Jobs in Cambridge
Sanofi/Wilkes Fellowship Program-Cambridge-
Job Description
Job Description
Program Overview
• The Fellow(s) will be a core member of the of Immunology & Inflammation (I&I) therapeutic area to support clinical development of immune-mediated disease treatments.
• The Fellow(s) will ensure...
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Editas Medicine-Cambridge-workable.com-
focus of this role is to lead medical and scientific strategic planning and operational execution of core medical affairs activities from early-clinical phase through lifecycle management for our lead in vivo development candidate, EDIT-401, a potential...
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Merida Biosciences-Cambridge-
Job Description
Job Description
Description:Sr. Director/Vice President of Clinical Development
At Merida Biosciences, we are pioneering true precision medicines for antibody-driven diseases. We specifically target pathogenic antibodies...
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Cambridge-tiptopjob.com-
and academic institutions to support the development of innovation for mutual benefit, and to help patients in all of our current therapy areas. Through a variety of partnership models, we accelerate ideas from the lab and clinic to advance and expand our...
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Scholar Rock-Cambridge-
of Position:
Scholar Rock is seeking an experienced and motivated Senior Director, Head of Clinical Quality Assurance to provide strategic and operational leadership for Good Clinical Practice (GCP) quality across the company’s biologics clinical development...
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Editas Medicine-Cambridge-workable.com-
focus of this role in the next 12 months is to advance our lead in vivo development candidate, EDIT-401, into the clinic by maintaining, enhancing, and supporting phase-appropriate quality systems and vendor management processes.
This role is part...
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Scholar Rock-Cambridge-
of Position:
The (Senior) Medical Director, reporting to the VP, Clinical Research, will be a member of the clinical research team, accountable for driving clinical development activities for assigned pipeline products.
The successful candidate...
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Editas Medicine-Cambridge-workable.com-
are desirable
• 10+ years of experience in biotech/pharma, with 8+ years in program management supporting early-stage clinical development. Experience managing multiple programs at the same time is desirable
• Solid understanding of science and experience...
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Scholar Rock-Cambridge-
in a clinical development program from clinical design to regulatory submission. The Biostatistics function is an integral part of every step of clinical development at Scholar Rock, and the Senior Manager/Associate Director, Biostatistics plays a key role...
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PhaseV-Cambridge-
Job Description
Job Description
PhaseV is a Boston-based technology company that redefines clinical development at scale with its enterprise-ready, multi-modal AI/ML platform — accelerating decisions, de-risking trials, and driving more efficient...
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Korro Bio-Cambridge-
delivery of high-quality, audit-ready clinical trial data in support of regulatory submissions and clinical development timelines. Acts as the primary data management point of contact for assigned studies/programs, overseeing CRO and vendor performance...
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AbbVie-Cambridge-
multimodal neurophysiological methodologies and translational utility. This role is an exciting opportunity to support psychiatry research from target validation, compound profiling, through clinical development in a dynamic, collaborative drug discovery...
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Tend-Cambridge-
expanded clinical leadership, market oversight, and performance impact. Market Lead Dentists are eligible for a monthly market performance bonus tied to clinical quality, provider development, and studio KPIs across their full market portfolio.
What You'll...
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Scholar Rock-Cambridge-
to the Senior Director, Head of Biomarker Development, this individual will support the discovery, development, and implementation of fit-for-purpose biomarker approaches that enable translation from discovery through early clinical development.
The Principal...
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Parabilis Medicines-Cambridge-
and a passion for process improvement. This role will partner closely with Regulatory Affairs, Medical Writing, Clinical Development, CMC, Quality, and external partners to ensure high-quality, compliant, and timely regulatory submissions.
Key responsibilities...
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