- Taiho Oncology (Princeton, NJ)
- Study Associate I, Clinical Operations...list, etc.). + Responsible for the review of the TMF plans to ensure consistency across studies and ... dynamic team cultivating growth and learning. Position Summary: The Study Associate (SA) I is responsible for...cross functional study team meetings and supports study manager with meeting minutes for assigned studies… more
- IQVIA (Parsippany, NJ)
- …other required study documentation. * Act as a mentor for clinical staff including conducting co-monitoring and training visits. * Collaborate and liaise with ... Overview Perform monitoring and site management work to ensure that sites are conducting the study (ies) and reporting study data as required by the study … more
- IQVIA (Parsippany, NJ)
- …Overview Perform monitoring and site management work to ensure that sites are conducting the study (ies) and reporting study data as required by the study ... with contracted scope of work and regulatory requirements, ie, Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. *… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …areas centered around rare diseases and immune disorders. **Summary:** The Associate Director, Laboratory Data Management is accountable for the end-to-end delivery ... of laboratory data in Daiichi Sankyo R&D collaborating with clinical and medical teams, clinical safety and...quality and time expectations for both in-house and outsourced studies . - Accountable for laboratory data management procedures and… more
- Daiichi Sankyo Inc. (Somerset County, NJ)
- …inspections of DM activity execution on clinical trials and review of the study TMF . Perform root cause analysis based on the findings from the inspections, ... areas centered around rare diseases and immune disorders. **Summary:** The Associate Director, Data Management Processes, Training and Inspection Readiness, is… more