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Today, Amylyx is a pharmaceutical company based in Cambridge, Massachusetts, that is dedicated to the discovery and development of potential treatments for diseases including Wolfram syndrome, progressive supranuclear palsy (PSP), and amyotrophic lateral sclerosis (ALS.
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The Regulatory Affairs Manager is responsible for managing RA submissions & Clinical Trials applications and will serve as a core member of the affiliate Regulatory Team interacting with local Regulatory Authorities and other stakeholders to ensure that the company complies with the country’s applicable legislations.
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At Collegium Pharmaceutical, we are building a leading, diversified specialty pharmaceutical company committed to improving the lives of people living with serious medical conditions.
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Performs duties as assigned by Pharmacy Manager, Staff Pharmacist and Store Manager including utilizing pharmacy systems to enter patient and drug information, ensuring information is entered correctly, filling prescriptions by retrieving, counting and pouring pharmaceutical drugs, verifying medicine is correct, and checking for possible interactions.
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Solid knowledge of the pharmaceutical environment and the role of medical affairs to advance the medical and scientific objectives of a pharmaceutical company. Screen relevant literature and other information from relevant scientific societies meetings and conferences and develop summaries of key messages for use within the company (e.g. key areas of scientific/company interest, new trends in diagnosis, monitoring and treatments in the therapeutic area, etc.
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We are a global diversified pharmaceutical company enriching lives through our relentless drive to deliver better health outcomes. Experience managing mid to large size projects in a complex matrixed medical device or pharmaceutical company or life sciences.
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Ph. D. in scientific field (e.g., pharmacokinetics, pharmacology, toxicology), with minimum of 10 years of leadership experience with nonclinical regulatory writing within a pharmaceutical company or Contract Research Organization (CRO.
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Experience in pharmaceutical or biotech product development across numerous modalities, with direct involvement in regulated studies related to pharmacology, toxicology, or pharmacokinetics, demonstrating a broad understanding of the drug development process.
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Ph. D. in Biological Sciences with 12 years of industry experience working in the pharmaceutical and/or biotechnology field as a biologist; or equivalent combination of higher education, training and experience.
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Join us on our journey of building a new kind of organization to reset expectations of what a bio-pharmaceutical company can be. 3+ years of proven experience defining and implementing the regulatory strategy for a pharmaceutical organization.
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Since our formation in 2019, when we carved out category leading brands from a Swedish pharmaceutical company, we've achieved remarkable growth. Advantice Health is a dynamic consumer health company that's passionate about improving skin health through science-backed, expert-loved solutions.
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Scientific Director, Global Scientific Communications - Gastroenterology and Rhinology (Dupixent/Itepekimab Alliance) We are an innovative global healthcare company, committed to transforming the lives of people with immune challenges, rare diseases and blood disorders, cancers, and neurological disorders.
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Doctoral degree (PhD., ScD or DrPH) in epidemiology (preferred) or a relevant discipline (i.e., health services research, health outcomes research, public health, statistics, or pharmaceutical sciences.
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T least 3 years of relevant experience in global patient recruitment, and clinical trial execution with a pharmaceutical company, CRO, and/or healthcare facility/research site. High degree of proficiency in Microsoft Excel, PowerPoint, and Word. Microsoft Project, Veeva preferred.
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Sebela Pharmaceuticals is a US pharmaceutical company with a market leading position in gastroenterology and a focus on innovation in women’s health. The QC Chemist will be responsible for performing testing of raw materials, in-process materials, and finished products to ensure compliance with established specifications and standards.
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pharmaceutical company jobs in Whitman, MA
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