- Takeda Pharmaceuticals (Providence, RI)
- …to bring life-changing therapies to patients worldwide. Join Takeda as an Associate Director , Global Regulatory Project Management and Strategic Planning - ... Regulatory Affairs Team. **How you will contribute:** + As Associate Director , Global Regulatory Project Management and Strategic Planning, you will… more
- Takeda Pharmaceuticals (Providence, RI)
- …You will serve as the regulatory expert for labeling on the Global Regulatory Affairs subteam to ensure that regulatory labeling requirements ... therapies to patients worldwide. Join Takeda as an Associate Director , Global Labeling Lead where you will...issues to Global Labeling management and the Global Regulatory Lead + Recommend strategies and… more
- J&J Family of Companies (Raynham, MA)
- …Clinical, Medical, Commercial and Professional Education, Communications and Regulatory . The Director of HEMA will work to ensure global market access ... and their team will develop health economic and outcomes studies to support the global businesses. Research activities conducted by the Director and their team… more
- Xerox (Providence, RI)
- …global guidelines, budgets, collateral materials for planning managers, global legal/ regulatory compliance, CEO approval process, participant communications). ... Director , Executive Compensation and Equity Administration **General Information**...plan service provider (Morgan Stanley). + Ensures compliance with regulatory and policy requirements (including Sarbanes Oxley… more
- Merck (Providence, RI)
- …including proportional hazards models. + Maintaining a comprehensive understanding of global regulatory expectations for small molecules and biologics in ... **Pharmacometrics -** **Immune/Oncology** **(QP2-IO)** team in the role of Director . QP2-IO team is part of the Global...+ Experience in IND, NDA and other submissions to global regulatory agencies. + Skills in experimental… more
- Merck (Providence, RI)
- …pharmacometric analyses + Developing and maintaining a comprehensive understanding of global regulatory expectations for small molecules and biologics, authoring ... development (MIDD) to routinely enable efficient drug discovery/development and/or regulatory decisions. The Pharmacometrics group within QP2 brings an experienced… more
- Merck (Providence, RI)
- …coaching/guidance to individual contributors. . Maintaining a comprehensive understanding of global regulatory expectations for small molecules and biologics, ... development (MIDD) to routinely enable efficient drug discovery/development and/or regulatory decisions. The Pharmacometrics group within QP2 brings an experienced… more
- Sumitomo Pharma (Providence, RI)
- **Executive Director , Commercial Supply Chain** Sumitomo Pharma America (SMPA) is focused on delivering therapeutic and scientific breakthroughs in areas of critical ... will be responsible for the oversight, management, and integration of the global commercial supply chain organization. This role will provide leadership and vision… more
- Merck (Providence, RI)
- …and Combination Product (MDCP) Quality Assurance Operations team, the Associate Director Quality Engineering & Quality Assurance is responsible for independent ... reviewing and approving medical device/combination product documentation to support regulatory filings and audits of data, policies, procedures, and systems… more
- Zurich NA (Providence, RI)
- VP, Corporate GL and Excess, Technical Director 113182 Zurich North America is currently looking for an experienced Commercial GL and Excess Technical Director . ... business travel expected. The Commercial GL and Excess Technical Director is responsible for managing a team, and establishing...book of business. S/he will work closely with our Global Colleagues and Business Unit Heads of Underwriting to… more