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To help provide a safe learning and living community, Wake Forest University conducts background investigations and drug screens for all final candidates being considered for employment. In order to provide a safe and productive learning and living community, Wake Forest University conducts background investigations and drug screens for all final staff candidates being considered for employment.
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Responsible for oversight of congress activity execution including development of digital materials, Medical Affairs exhibit booth planning, HCP engagement strategy, insight generation, educational programs such as scientific symposia while ensuring alignment with educational objectives.
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Create the clinical development strategy for one or more assets and document it in the clinical development plan in collaboration with the global project team and internal partners such as clinical operations, translational medicine, regulatory affairs, biostatistics, drug discovery, drug safety, marketing.
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The ASR includes crime statistics and institutional policies concerning campus security, such as those concerning alcohol and drug use, crime prevention, the reporting of crimes, sexual assault, and other matters.
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Develop or review all key pursuit strategy and positioning, and lead or support proposal development. All applicants must be able to complete pre-employment onboarding requirements (if selected) which may include any/all of the following: criminal/civil background check, drug screen, and motor vehicle records search, in compliance with any applicable laws and regulations.
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Nuvalent is an exciting early-stage company, bringing together experienced scientists and industry veterans with a proven track record in drug discovery, oncology drug development, and company building.
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The ideal candidate will have experience in implementing AI/ML in biopharmaceutical R&D (specifically within drug discovery, process development, bioanalysis, or manufacturing) and deeply understands how AI/ML can potentially address our customers' most important problems and drive superior business outcomes.
$219,980 - $297,620 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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As a senior clinical development team member, the incumbent will lead the successful delivery of milestones for assigned project(s), such as IND, EOP2, NDA and MAA for the company, drawing on expertise in clinical and regulatory strategy and requirements, both local and international, related to the clinical medicine and drug development processes.
$155,000 - $264,000 a yearFull-timeRemoteExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Senior director, clinical program lead, late-stage clinical development, clinical trials, global, strategy, hematology, lymphoma, oncology, targeted therapies, ADCs, antibody-drug conjugates, program, asset, label extension, life-cycle management, pharma, biotech, biopharma, MD, medical doctor, phase I, phase II, phase III, FDA.
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As the Senior Regulatory Affairs Specialist, you will support product development activities on cross-functional project teams for both US and OUS global regulatory release by contributing to the development and updating of regulatory strategy.
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The ideal candidate must have a strong desire to support the Sustainability Solution group's business vision - which is to be the leading sustainable consulting and EPC firm - by supporting projects with the strategy, concepts and insights, analytical techniques, implementation capabilities in the energy industry and adjacent sectors.
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Proven experience in hematology/oncology drug development, designing and managing clinical trials (Ph 1b/II and Ph III) through investigator and regulatory interactions; experience with early-clinical development, including FIH and IND, is a plus.
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Senior Director, Late-stage Clinical Development | MD Leadership | Successful Commercial Hematology/Oncology Biotech | Great Culture | REMOTE/HYBRID role. Strong ability to partner with other functions, including preclinical, early-stage clinical development, clinical operations, regulatory, and external collaborators.
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Knowledge of the drug development process. We do this through strategic and complimentary areas of focus: Asset Optimization and Commercialization, Value, Access, and Outcomes, Medical Strategy and Communications, and Real-World Evidence.
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This company is a global leader in antibody-drug conjugates, with multiple ongoing studies for hematologic and solid tumor cancers. This Physician will lead clinical studies focusing on specific indications/label extensions or a whole development program until filing, and further for life cycle management.
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