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This includes organizing, assigning, and overseeing key preclinical and clinical experimental projects in support both compound specific programs and on broader clinical translational research scientific projects.
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Support project teams, regulatory affairs, product management, marketing, and product stewardship in topics related to toxicology and kinetics. You will represent Toxicology & Kinetics in international cross-functional teams and contribute to the dsm-firmenich innovation strategy by supporting Research & Development projects during the entire project life cycle.
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The successful candidate will have prior therapeutic area and late development clinical experience in biotech/pharma organizations interacting with project teams, clinical research physicians, statisticians, computational biologists, contract research organizations and translational scientists to deliver science that supports the development of medicines to patients in need.
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The Program on Science and Global Security (SGS), part of the Princeton School of Public and International Affairs (SPIA), seeks to hire a Program Manager to work with Program leadership, faculty members and researchers on projects related to scientific, technical and policy research, analysis and outreach to advance national and international policies for a safer and more peaceful world.
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Associate Director, Global Regulatory Affairs Operations, Authoring Support page is loaded. The Team Lead for Authoring Support Group will be part of the Global Regulatory Operations group and will develop and manage the authoring support group within Regulatory Affairs (RA) to ensure timely and high-quality document delivery to the Regulatory Publishing Group.
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Designs and develops clinical studies and research plans in support of asset strategy with the Early Clinical Development Leadership team; clinical studies include first-in-human Phase I, proof of concept Phase I/II, entry registrational studies, biomarker qualification studies, and/or clinical pharmacology studies.
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Ability to interpret complex research documents, write scientific reports, communicate abstract concepts, and present to high-level audiences. We are seeking a Pharmacologist/Toxicologist Lead with a strong scientific background to join our team, based remotely in Princeton, NJ. This role plays a crucial part in applying scientific methodologies to overcome challenges in pharmacology and toxicology, leading developmental programs, conducting risk assessments, and representing the company in meetings with global health authorities.
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Manage pre-clinical activities for drug candidates through IND enabling studies in close collaboration with Translational Research, Toxicology, DMPK, and other functions. For more than 20 years, its passionate, innovative and collaborative team has invented next-generation antibody technology platforms and leveraged translational research and data sciences, which has resulted in a proprietary pipeline including bispecific T-cell engagers, next-generation immune checkpoint modulators, effector function enhanced antibodies and antibody-drug conjugates.
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Ability to work closely with HCPs in the rare disease space and provide valuable scientific exchange specifically in Rett Disease including clinical research, patient and caregiver burden, disease landscape and payer value.
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PhD or MS in Life Sciences with at least 5 years of relevant experience in clinical science, clinical research or other relevant scientific field. The Associate Director, Bioanalysis, Genomics & Biomarker Research manages outsourced measurement in biological fluids to support clinical drug development and analyzes complex datasets through computational genomics and bioinformatic pipelines.
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The Scientific Director will serve as a leader in and provide strategic insight to the Medical and Scientific Services department and oversee the development of technically accurate and high-quality deliverables for Medical Education accounts.
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Work From Home, Entry Level Data Entry Clerk As A Research Participant. We need folks who want to do tasks, micro tasks, work at home opinion panels, online focus groups, product testing, research trials and more.
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Deep understanding of pharmaceutical research and development (R&D) and commercialization processes is necessary, as is an in-depth knowledge of the principles and practices of pharmaceutical clinical studies, including study design, conduct, analysis, and reporting.
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The Clinical Nurse 2 or Clinical Nurse-NCL demonstrates within the competency domains of Continuous Quality Improvement, Evidence Based Practice and Research, Leadership, Person and Family Centered Care, Professionalism, Safety, Technology/Informatics, and Teamwork.
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Work closely with a cross disciplinary team of data scientists, structural biologist, and computational biologists, imaging experts, and leverages cross-domain expertise to contribute to a rigorous scientific evidence package strategically aligned with the drug discovery needs and strategy.
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clinical research scientific affairs jobs Title: director Company: Regeneron Pharmaceuticals Inc in Lawrence, NJ
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