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Relationships Reports to the Senior Director, Clinical Pharmacology for the U.S. East Coast Hub. Will interact with Medical Specialists, Clinical Operations, Medical writing, Regulatory, Data Science (statistics, pharmacometrics), Research and Early Development, Global Translation, Global Medical Affairs, Global Safety (GS), Bioanalysis, CMC and occasionally with leadership in Medical and Science.
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The Director, Medical Affairs Rare Disease (ELA) will provide support to all US Medical Affairs activities related to the Rare Disease- Liver portfolio. Minimum of 10 years’ experience in the biotech/pharmaceutical industry and/or relevant experience with at least 7 years in Medical Affairs Hepatology and/or Rare Disease experience.
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The Government Relations Manager is responsible for leading and coordinating CLF’s Massachusetts state legislative advocacy and relationships with state agencies including the Executive Office of Energy and Environmental Affairs and the Department of Environmental Protection.
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As the Quality Systems Lead, you are a seasoned individual in the field of GMP commercial and clinical phase manufacturing supply with a background in quality and regulatory compliance. As MEDIPOST embarks on a journey to halt degenerative diseases such as osteoarthritis, we are seeking a talented and experienced Director of Quality Systems who will ensure that DS and DP production for our Phase III trials and commercial supply are compliant with current quality and regulatory standards.
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Drafts, reviews and negotiates commercial, clinical, and other contracts and agreements. Ensures compliance with other legal/regulatory requirements, including anti-bribery/anti-corruption, global trade, data privacy, healthcare.
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The Director, Bioanalytical Diagnostic Development, will be responsible for defining the global bioanalytical development strategy and leading all activities related to clinical bioassays/diagnostics, from preparations for ‘first in human’ up to registrational studies and post-approval commitments.
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Generation Bio is seeking an energetic and highly motivated Associate Director/Principal Scientist to join the Immunology Group. Design and execute in vivo pharmacology studies in WT and disease models.
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Position Summary The Director, CPQP position resides within Alexion’s Clinical Pharmacology and Safety Sciences (CPSS) organization. The role represents the CPQP function on drug development teams, leads CPQP sub-teams, and owns strategy and delivery on posology for early and late-stage clinical trials while collaborating with clinicians, clinical operations, bioanalytical, biomarker, pharmacovigilance, regulatory and CMC groups.
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The role requires a strong ability to work independently while collaborating with the desk and other IT teams at BETM. This position will report to the head of IT Team and will be located either in our Boston, MA office.
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Join Takeda as a Director of Cell Therapy where you will lead a team responsible for designing and implementing in vitro pharmacological assays, using state-of-the-art technologies and methodologies, leading the discovery of novel Cell Therapy products, and contributing to the strategic direction of our Cell Therapy research programs.
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Associate Director/Director, Medicinal Chemistry. Build and maintain productive relationships with internal and external collaborators in biology, pharmacology, computational chemistry, DMPK, toxicology, and early development.
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Master's Degree in College Student Personnel, Student Affairs, Psychology, or a related field required. Depending on building assignment, the Residence Director will report to either the Associate Director, Residential Education or the Assistant Director, Residential Education.
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The candidate will report to the Executive Director for Global Corporate Affairs Alzheimer’s disease, with additional accountability to the International Therapy Area Leader. The Associate Director of Corporate Affairs (CA) for Alzheimer's disease will play a crucial role in supporting both the development and implementation of international strategies to improve the detection, diagnosis, and care of Alzheimer's disease.
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Job Overview: The Medical Director will oversee the medical strategy and clinical development for immuno-oncology programs, ensuring alignment with company objectives. Oversee and direct the medical strategy and clinical development for immuno-oncology programs.
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The Strategy Director is an integral contributor to the development, governance, and realization of John Hancock’s long -term strategy and vision. Manulife/John Hancock offers eligible employees a wide array of customizable benefits, including health, dental, mental health, vision, short- and long-term disability, life and AD&D insurance coverage, adoption/surrogacy and wellness benefits, and employee/family assistance plans.
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affairs job Title: director clinical assoc in Waltham, MA
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