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Reporting to the Chief Development Officer, the VP, Drug Safety & Pharmacovigilance will be responsible for leading the overall strategic direction for Safety and Pharmacovigilance and, through leadership of the team, oversee the operational delivery of safety and pharmacovigilance activities at Bicycle.
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Collaborate with senior executives to integrate drug safety & pharmacovigilance considerations into overall business strategies, clinical development plans, and broader decision-making processes.
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Must have a thorough knowledge of clinical research concepts, practices, and FDA regulations and ICH Guidelines regarding drug development phases, clinical trials, clinical study design, and data management methods.
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Lead the translational aspect of drug discovery, ensuring seamless progression of immunology projects through all phases of clinical development. Job Overview: This role will lead the development of innovative oral degrader programs and oversee translational immunology and Inflammation projects, applying your expertise in immunology and Inflammation to drive progress and decision-making across our clients portfolio.
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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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Deep knowledge of external landscape, drug development, and path to commercialization. 15+ years progressive Biopharmaceuticals experience, with a background in rare disease development.
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The successful candidate will play a critical role in the strategy and execution of Acrivon’s biomarker-driven clinical development through co-development of our pioneering drug-tailored predictive biomarker tests and working closely with the Acrivon biomarker platform team to unlock the value and promise of our precision medicines in oncology and beyond.
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REQUIRED : Strong knowledge and experience with of small molecule nonclinical development, drug metabolism, ADME concepts, pharmacokinetics, pharmacodynamic and bioanalytical principles. The ideal candidate will possess a unique blend of scientific expertise, strategic acumen, and leadership prowess, guiding cross-functional teams through the landscape of drug development.
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Desired: Expertise in the fundamentals of drug development, including pharmacology and DMPK. Deep knowledge of formulation discovery, biotechnology/pharmaceutical development, and delivery of novel drug modalities.
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Ph. D. in Pharmaceutical Science and 15+ years of experience in the pharmaceutical industry in roles of increasing responsibility, or equivalent in Chemistry or Biological science with drug or radiopharmaceutical agent development.
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At least 10 years of experience in oncology clinical pharmacology, with a significant track record in clinical drug development in an industry setting. Participate in the advancement of drug candidates from preclinical development, ensuring seamless transitions into clinical trials.
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Vice President, Immunology and Inflammation 2031144. We offer quality career resources, training, certifications, development opportunities, and a comprehensive benefits package. PhD or MD/PhD in Immunology, Inflammation or a closely related field coupled with at least 15 years of experience in both preclinical and clinical immunology research, including a leadership role in project management, and a preference for clinical laboratory medicine exposure.
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Expertise in synthesizing significant data spanning multiple functional areas, and balancing drug discovery and development decisions with strategic business sense. The VP, Corporate Partnerships and Program Development will contribute to strategy and execution of business development and collaboration innovation across the Flagship ecosystem.
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Provide Translational Medicine and Immunology leadership to multiple drug discovery programs in Kymera's immunology pipeline, driving translational projects from discovery into early and late clinical development.
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What You’ll Do: The Vice President of Chemistry, Manufacturing, and Controls (CMC) is responsible for leading and overseeing all aspects of the CMC function, ensuring the successful development, manufacturing, and regulatory approval of biopharmaceutical products.
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drug development jobs Title: vice president in Lexington, MA
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