- J&J Family of Companies (Titusville, NJ)
- …with excellent knowledge and understanding of design control process, analytical and clinical validation, manufacturing, GCP , GLP, and GMP requirements, Global ... for humanity. Learn more at https://www.jnj.com **Job Function:** Discovery & Pre- Clinical / Clinical Development **Job Sub** **Function:** Clinical … more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …and external stakeholders to optimize processes, technology, and standards. This position ensures quality delivery of data for clinical trials, clinical ... regulatory submissions. This position develops and proposes strategies for ensuring all clinical trials meets quality requirements and best practices. This… more
- Amgen (Washington, DC)
- … clinical trial design, including biostatistics + Knowledge of Good Clinical Practices ( GCP ), region regulations and guidelines, and applicable international ... Join us and transform the lives of patients while transforming your career. **Medical Director - Medical Affairs - TAVNEOS** **What you will do** Let's do this.… more
- Regeneron Pharmaceuticals (Armonk, NY)
- …in Clinical Trial Management (CTM). This individual is responsible for clinical operations activities and decisions including quality , timelines and budgets ... clinical research studies in accordance with applicable regulations, ICH/ GCP regulations and company Standard Operating Procedures (SOPs) within assigned… more
- Regeneron Pharmaceuticals (Cambridge, MA)
- …in Clinical Trial Management (CTM). This individual is responsible for clinical operations activities and decisions including quality , timelines and budgets ... clinical research studies in accordance with applicable regulations, ICH/ GCP regulations and company Standard Operating Procedures (SOPs) within assigned… more
- Otsuka America Pharmaceutical Inc. (Annapolis, MD)
- **Job Summary** Under the direction of the Director /Associate Director of Clinical Management, the Senior Clinical Study Manager is responsible for the ... trials according to applicable regulations and guidance; ICH Guidelines Good Clinical Practices ( GCP ), and Otsuka SOPs, within agreed-upon timeframes and… more
- Amgen (Washington, DC)
- …in matrixed, cross-functional teams and leading external partnerships + Knowledge of clinical trial design, GCP , and regulatory pathways for biomarker and ... and transform the lives of patients while transforming your career. **Senior Director , Precision Medicine Therapeutic Area Lead - Cardio/Metabolic** **What you will… more
- Translational Research in Oncology (Washington, DC)
- If you are an experienced Senior Clinical Quality Assurance Auditor (internally referred to as Senior Clinical Quality Assurance Manager) who is ... the world of today. TRIO is seeking a Senior Clinical Quality Assurance Auditor (internally referred to... Quality Assurance Manager) to join our Quality Assurance team. Reporting to the Senior Director… more
- IQVIA (Durham, NC)
- …knowledge of standard operating procedures (SOPs), Good Clinical Practice ( GCP ), Food & Drug Administration (FDA) regulations, quality improvement ... of R&DS Business: commit to customer success, delivery with exceptional quality every time, differentiate with therapeutic expertise, science, & technology, and… more
- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- … clinical research studies in accordance with applicable regulations, ICH/ GCP regulations and company Standard Operating Procedures (SOPs) within assigned ... is responsible for leadership and overall strategic management of Programs in Clinical Data Management (CDM). This individual is responsible for data management… more