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Week)Frontage Laboratories Inc. is an award winning, publicly listed (HKSE), full-service CRO/Contract Research Organization operating over 25 state-of-the-art laboratories across the US, Canada, and China, and growing over 30% YOY. Our core competencies include drug metabolism, pharmacokinetics/ pharmacodynamics (PK/PD), safety and toxicology, bioanalytical services, chemistry and manufacturing controls for drug development, and core laboratory services for clinical trials.
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Perform assay development, validation, and sample bioanalysis for preclinical and clinical studies. + at least 1 year of knowledge and hands-on experience in LBA such as ELISA and the application to drug or biomarker concentration measurement as evidenced by laboratory skills.
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Provide regulatory guidance to drug development teams, merging scientific principles and FDA law and regulations for development of marketing materials. Description About the role:Join Takeda as a Senior Manager, US Medical Ad/Promo Regulatory Review where you will serve as an internal expert on FDA regulations, guidance, and enforcement trends governing the promotion of prescription drug and biologic products.
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The Senior Program Management (Early-Stage Development) will partner with the Development Program Lead (DPL) to lead the Development Program Team (DPT) to successfully shape and execute the project and drug development strategies, as well as, lifecycle plan.
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The company’s product portfolio includes coatings, drug delivery platforms, mechanical devices, and a wide range of biomedical materials that enable the replacement, repair, enhancement and the regeneration of tissue and organ functions in the body.
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Founded in 2004, Pharmaron has invested in its people and facilities, and established a broad spectrum of research, development and manufacturing service capabilities throughout the entire drug discovery, preclinical and clinical development process across multiple therapeutic modalities, including small molecules, biologics and CGT products.
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Job Summary The Corporate Development team plays a crucial role in driving the strategic growth agenda of the company through various initiatives including mergers and acquisitions (M&A), partnerships, joint ventures, and strategic alliances.
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Provide regulatory guidance to drug development teams, merging scientific principles and FDA law and regulations for development of marketing materials, including representation on global regulatory and labeling teams.
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Preferred: Experience in Gx and Biosimilar drug development. The PM will work in partnership with a Program Leader to establish, maintain and deliver the priority product plan for all development stages.
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Employment with Sunrise is conditioned on completing and passing a drug test (which does not include marijuana), participating in testing requirements (e.g. Tuberculosis Test, Physical Evaluation.
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PCI is seeking an experienced Business Development Manager for its Cleanroom Contracting Group based out of our PCI Philadelphia operations located in Exton, PA. PCG is a background screening, drug-free workplace.
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Essential Duties and Responsibilities: Technical packaging lead for R&D efforts related to product design and development processes from conceptualization to commercialization. Where permitted by law, employment with West Pharmaceutical Services, Inc. or any of its subsidiary or affiliate companies, is contingent upon the satisfactory completion of post-offer background screening and/or drug screening.
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Drug Product Development | 6 Months Co-Op| Start date Jan 6th - June 2025. General knowledge of drug product development. Support the fill/finish team with recipe development, execution, and standardization of vial fills.
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Frontage Laboratories Inc. is an award winning, publicly listed (HKSE), full-service CRO/Contract Research Organization operating over 25 state-of-the-art laboratories across the US, Canada and China, and growing over 30% YOY. Our core competencies include drug metabolism, pharmacokinetics/ pharmacodynamics (PK/PD), safety and toxicology, bioanalytical services, chemistry and manufacturing controls for drug development, and core laboratory services for clinical trials.
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Minimum 8 years of experience as Account Manager/Business Development Manager/Sales Team Manager supplying Drug Product Manufacturers. Understand the customer’s business and product development strategies by segment to assure that West is positioned as the preferred choice for new products.
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drug development jobs in Exton, PA
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