- Takeda Pharmaceuticals (Providence, RI)
- …is possible in order to bring life-changing therapies to patients worldwide. Join Takeda as Senior Manager , Global Regulatory Labeling Strategy where you ... Coordinates the process to obtain labeling approval by Labeling Senior Management Cross-functional team ( Global Labeling Oversight...issues to Global Labeling management and the Global Regulatory Lead (GRL) and proposes risk… more
- Takeda Pharmaceuticals (Providence, RI)
- …in order to bring life-changing therapies to patients worldwide. Join Takeda as the Senior Manager , Global Labeling Devices. You will be responsible for ... Serve as the expert for device labeling on the global Regulatory Affairs (RA) Sub team and...the process to obtain IFU labeling approval by Labeling Senior Management Cross-functional team ( Global Labeling Oversight… more
- Sumitomo Pharma (Providence, RI)
- …leadership in the design, analysis, and reporting of clinical studies. The Senior Manager will collaborate with cross-functional teams to ensure statistical ... a dynamic, highly motivated, and experienced individual for the position of ** Senior ** ** Manager , Biostatistics.** This role will support clinical development… more
- Takeda Pharmaceuticals (Providence, RI)
- …company to inspire you and empower you to shine? Join us as a Senior Manager , Integrated Clinical Trial Data Process Excellence and Delivery based remotely ... be a necessary contributor to our inspiring, bold mission. **_GOALS:_** + The Senior Manager , Process Excellence and Delivery supports the strategy to develop… more
- Sumitomo Pharma (Providence, RI)
- …currently seeking a dynamic, highly motivated, and experienced individual for the position of ** Senior Manager , Clinical Trials.** The Senior Manager , ... Sumitomo Pharma Co., Ltd. is a global pharmaceutical company based in Japan with key...operational aspects for clinical studies across Phase 1-4. The Senior Manager , Clinical Trials will work under… more
- Sumitomo Pharma (Providence, RI)
- …to planning, executing, and problem solving + Working knowledge of current global regulatory requirements and guidelines for clinical trials. **Education and ... Sumitomo Pharma Co., Ltd. is a global pharmaceutical company based in Japan with key...and ensures the documentations are in accordance with GCP regulatory requirements and consistent with the protocol for assigned… more
- Takeda Pharmaceuticals (Providence, RI)
- …true to the best of my knowledge. **Job Description** Objective / Purpose: The Senior Manager Clinical Data Management is responsible for timely and high quality ... ICH-GCP and Takeda's Scope of Work, maximize effectiveness and maintain budgets. The Senior Manager Clinical Data Management provides and enables solutions for… more
- Fujifilm (Providence, RI)
- **Position Overview** The Senior Project Manager , SDS manages, leads, and coordinates all aspects of the Synapse MI implementation process from quotation to ... and smiles for various stakeholders as a collection of global leading businesses and achieve a global ...the position. + Adheres to the Company's quality and regulatory compliance requirements, without exception, and ensures that all… more
- Sumitomo Pharma (Providence, RI)
- …seeking a dynamic, highly motivated, and experienced individual for the position of ** Senior Manager , Medical Affairs Technology and Digital Innovation** . **Job ... Sumitomo Pharma Co., Ltd. is a global pharmaceutical company based in Japan with key...role requires experience with commercial organizations, legal, medical and regulatory needs as well as internal pharmaceutical and biotechnology… more
- Takeda Pharmaceuticals (Providence, RI)
- …safety reporting requirements + Ensureoverall performanceofthedepartmentand compliance with global regulatory requirements by implementation of appropriate ... according to company timelines and quality standards + Oversee regulatory submissions for ICSRs from the Global ...Oversee regulatory submissions for ICSRs from the Global Safety database, on-time delivery of adverse event reports… more