At Genmab, we are dedicated to building extra[not]ordinary® futures, together, by developing antibody products and groundbreaking, knock-your-socks-off KYSO antibody medicines® that change lives and the future of cancer treatment and serious diseases. We strive to create,
When our values align, theres no limit to what we can achieve. At Parexel, we all share the same goal - to improve the worlds health. From clinical trials to regulatory, consulting, and market access, every
Job Description General Summary: The Project Management and Strategic Operations Director leads large-scale, high-value CMC programs end to end, setting a high standard for decision quality, governance, risk management, and execution. This role combines deep program management
At Genmab, we are dedicated to building extra[not]ordinary® futures, together, by developing antibody products and groundbreaking, knock-your-socks-off KYSO antibody medicines® that change lives and the future of cancer treatment and serious diseases. We strive to create,
Your work will change lives. Including your own. The Impact You’ll Make Lead development and implementation of CMC regulatory strategy for small molecule investigational drugs in global Phase 1-3 clinical trials and marketing applications. Influence the regulatory
Your work will change lives. Including your own. The Impact You’ll Make Lead development and implementation of CMC regulatory strategy for small molecule investigational drugs in global Phase 1-3 clinical trials and marketing applications. Influence the regulatory
General Information Job Advert Title: 【アステラス製薬/焼津】経口製剤処方およびプロセス設計担当（主に低／中分子医薬品，グローバルCMC） Location: Yaizu, Shizuoka Division: Product Research & Development Employment Class: Permanent Description 【募集の背景 / Purpose & Scope】 アステラス製薬製剤研究所では患者さんの「価値」向上のため，患者さんに実際に投与し，最大限の効果を発揮できる製剤化研究を実施しています。治療手段，モダリティが多様化する中でも，経口製剤は治療手段として引き続き重要な位置を占めています。製剤開発研究室では，主に経口製剤の開発において，処方設計・プロセス設計あるいは生産サイトへの技術移転・商用生産等の経験を有し，斬新なアイデアとチャレンジ精神，熱意を持って製剤研究や新規技術開発を遂行し，プロジェクトをグローバルにリードできる人材を募集します。 【職務の内容 / Essential Job Responsibilities】 （雇入れ直後） チームリード，製剤リードの指示のもと，経口剤の開発を中心に下記の業務を遂行していただきます。 ・ 経口剤の処方設計 ・ 経口剤の治験薬製造 ・ 経口剤のプロセス開発（スケールアップ検討含む）
At Allucent, we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need across the globe. We are looking for a Sr. Director,
At Genmab, we are dedicated to building extra[not]ordinary® futures, together, by developing antibody products and groundbreaking, knock-your-socks-off KYSO antibody medicines® that change lives and the future of cancer treatment and serious diseases. We strive to create,
Join our team in a dynamic hybrid role, offering flexibility to work remotely and from our headquarters in Watertown, MA. COMPANY OVERVIEW: Disc Medicine is a clinical-stage biopharmaceutical company committed to discovering, developing, and commercializing novel
Build our future together: As an Associate Director you will lead the development and execution of global CMC regulatory strategies for the hematology and oncology portfolios. You will guide regulatory activities across development stages, mentor CMC Regulatory Affairs
Build our future together: As an Associate Director you will lead the development and execution of global CMC regulatory strategies for the hematology and oncology portfolios. You will guide regulatory activities across development stages, mentor CMC Regulatory Affairs
Job Description SummaryWe are seeking a highly motivated and detail-oriented Regulatory Affairs – CMC professional with a strong background in radiopharmacy or radiopharmaceutical development. The successful candidate will support global regulatory strategy and execution for both marketed
If it’s possible, you will find it at Atrium Health—the leading community-focused academic healthcare system serving North Carolina, South Carolina, and Georgia. We invite Physician Assistants and Acute Care Nurse Practitioners to discover all that we
Axsome Therapeuticsis a biopharmaceutical company leading a new era in the treatment of central nervous system (CNS) conditions. We deliver scientific breakthroughs by identifying critical gaps in care and develop differentiated products with a focus on
Department: 10169 Enterprise Corporate - Clinical Documentation Improvement Status: Full time Benefits Eligible: Yes Hours Per Week: 40 Schedule Details/Additional Information: Weekdays Pay Range$38.20 - $57.30 Job Summary Assists treating providers to ensure documentation in the
Company Description Are you looking to join an organization that is growing and dynamic? What about a high-energy, collaborative environment that rewards hard work? J.S. Held is a global consulting firm that combines technical, scientific, financial,
About GenScript GenScript Biotech Corporation (Stock Code: 1548.HK) is a global biotechnology group. Founded in 2002, GenScript has an established global presence across North America, Europe, the Greater China, and Asia Pacific. GenScripts businesses encompass four
Join us as we transform immunology and deliver medicines that help autoimmune patients get their lives back. argenx is preparing for multi-dimensional expansion to reach more patients through a rich pipeline of differentiated assets, led by
SUMMARY Review clinical documentation and diagnostic results to extract data and apply appropriate ICD-10-CM and ICD-10-PCS codes for billing, internal and external reporting, research, and regulatory compliance. Demonstrate knowledge of reimbursement methodologies and apply these to