- Daiichi Sankyo, Inc. (Bernards, NJ)
- …and immune disorders. Job Summary: Assist in planning and execution of clinical studies , under the supervision of the Study Manager role the Study ... to monitor and ensure compliance with Daiichi Sankyo Clinical Study Oversight Plan (CSOP).Responsibilities:Reconcile the TMF document trackers generated by… more
- Daiichi Sankyo, Inc. (Bernards, 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 pharmacovigilance, CROs and other vendors to ensure… more
- 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 (New York, NY)
- …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 ... in accordance with contracted scope of work and Good Clinical Practice. * Work with sites to adapt, drive,...needs to enhance predictability. * Administer protocol and related study training to assigned sites and establish regular lines… 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
