- Vitalief (New Brunswick, NJ)
- …Join us and help clients adapt to evolving requirements in the research and clinical trial industry with cutting-edge solutions. Reasons to Work for Vitalief: + ... and managing patient care (patient retention). + Assist with monitoring patient visits. + Track deviations and documenting SAEs...of experience in Clinical Research as a Clinical Research Coordinator , with experience in patient… more
- J&J Family of Companies (Trenton, NJ)
- …of documentation needed for internal and external audits to ensure all essential clinical Trial Master File (TMF) documents are compliant with Good Documentation ... parameters of study hypothesis, as well as to monitor clinical trial /study safety, in keeping with protocols,...+ Clinical research certification (ACRP or SoCRA, Clinical Coordinator /CRA certification) **Other:** + Must upload… more
- Merck (Trenton, NJ)
- …The CQOM will oversee headquarters clinical quality operations and support clinical trial teams within the assigned therapeutic area, to proactively embed ... Categorization Tools and Quality Plans in partnership with the Clinical Trial Team (CTT). + Collectively and...include, but not be limited to: 1) Facilitating and monitoring CTT oversight of vendors; 2) Development, review and… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …and International Conference on Harmonization (ICH) guidelines. Key focus is on providing clinical trial management support to study teams and tracking CRO and ... rare diseases and immune disorders. **Summary** Assist in planning and execution of clinical studies, under the supervision of the Study Manager role the Study… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …and International Conference on Harmonization (ICH) guidelines. Key focus is on providing clinical trial management support to study teams and tracking CRO and ... rare diseases and immune disorders. **Summary** Assist in planning and execution of clinical studies, under the supervision of the Study Manager role the Study… more