- J&J Family of Companies (Titusville, NJ)
- …or submission related work based on area of responsibility. The Senior Manager , RA Submissions makes decisions that impact CTA submissions that will be ... Belgium; Allschwil, Switzerland; High Wycombe, Great Britian; Leiden, Netherlands) **Purpose:** The Senior Manager , RA Submissions is a member of the … more
- Otsuka America Pharmaceutical Inc. (Bismarck, ND)
- …pharmaceutical and/or healthcare industry. - Knowledge and experience with preparation of global regulatory submissions (IND, CTA , NDA or BLA, MAA). - RAC ... **Position Summary** Provides critical support in developing global regulatory strategy, planning and execution of global investigational and marketed prescription… more
- Chicago Transit Authority (Chicago, IL)
- Manager , Administration - Rail Station Management - ( 25000062 ) **Description** **SALARY** $110,872.59 **POSITION SUMMARY** Supervises and coordinates budgetary, ... documents and/or information as requested. + Monitors various safety and regulatory requirements and recommends appropriate training programs to keep employees… more
- Deloitte (Detroit, MI)
- …resilience, grow with confidence, and proactively manage to secure success. We are seeking a Senior Manager to join our team and play a pivotal role in advancing ... develops and transforms cyber programs in line with a client's strategic objectives, regulatory requirements, and risk appetite. It keeps the enterprise a step ahead… more
- BeOne Medicines (San Mateo, CA)
- **_General Description:_** BeOne is seeking an experienced and energetic regulatory professional to manage, evaluate, and complete regulatory projects consistent ... responsible for development of strategies, planning, drafting, and managing CMC-related regulatory submissions and HA interactions to meet the aggressive timelines… more
- Amgen (Washington, DC)
- …us and transform the lives of patients while transforming your career. Biostatistics Sr Manager **What you will do** Let's do this. Let's change the world. In this ... the clinical development environment with the supervision of more senior staff. **Accountabilities** *Provide dedicated support for Exploratory Biostatistics… more
- Pfizer (Sacramento, CA)
- …Management (SUPM), Site Activation Partner (SAP), Clinical Trial Assistant ( CTA ), Investigator Contracts Lead (ICL), Site Monitoring, Optimization, Analytics, and ... to country and site selection and collaborate with country regulatory /regional Clinical Trial Regulatory Operations (CTRO) to...as described in the Site Care Partners & Line Manager of SCPs job description and ensure compliance with… more