- Amgen (Washington, DC)
- …and transform the lives of patients while transforming your career. Clinical Research Medical Director, Uplizna **What you will do** Let's do this. Let's change the ... knowledge into the development, delivery and communication of the global scientific/ medical evidence plan for the indication(s). + Provide oversight of LCM… more
- United Therapeutics (Research Triangle Park, NC)
- …transplant is not currently an option. The Senior Project Manager of Medical Affairs will independently provide oversight and coordinate the operational delivery of ... and other relevant functional groups (UT and / or CRO ) to manage and engage with clinical study sites,...GCP/ICH regulations and guidelines + Strong overall scientific and clinical/ medical research background + Experience with EDC and CTMS… more
- Charles River Laboratories (Reno, NV)
- …you can feel passionate about. **Job Summary** **BASIC SUMMARY:** Perform basic medical technology procedures according to protocol, SOP and GLP. Operate, maintain ... protocol work schedule for each study, as needed. * Perform basic medical technology procedures such as record blood slide differentials, reticulocyte counts, and… more
- Otsuka America Pharmaceutical Inc. (Boise, ID)
- **Job Summary** Otsuka is looking for a strong Clinical Statistician in the Medical and Real World Data Analytics organization to provide statistical expertise for ... internal data scientists and data programmers, and external stakeholders including Medical Affairs, Value and Real World Evidence to provide end-to-end statistical… more
- IQVIA (Washington, DC)
- MCRA is part of IQVIA MedTech. As a trusted CRO and advisory partner, IQVIA MedTech and MCRA deliver integrated lifecycle solutions for the medical device and ... May perform and plan the programming of database quality control checks. * Program and plan the integration of...related field and 4 years relevant experience Req * Medical device experience preferred. * SAS Certified preferred. *… more
- BeOne Medicines (Emeryville, CA)
- The Executive Medical Director will support BeOne Clinical and Medical assets within the Hematology franchise by successful development of early and late phase ... expertise for selection of investigator and vendors. + Provide scientific and medical support throughout conduct of a clinical trial; respond to clinical questions… more
- Pfizer (Cambridge, MA)
- …selection, qualification, performance evaluation, periodic visits and audits of CRO laboratories conducting clinical biomarker assays. Assists CROs with effective ... SME. + May consult on CRC studies and research initiatives managed by Medical Affairs. + Works with biomarker and clinical teams to interpret biomarker results… more
- J&J Family of Companies (Titusville, NJ)
- …reporting by creating data visualizations and listings for data management, medical monitoring, and central monitoring. Principal Relationships: + This role reports ... and Central Monitoring, Programming Leads, Clinical Data Standards, Regulatory Medical Writing Leads, and system support organizations. + Functional Contacts… more
- IQVIA (Durham, NC)
- …Sales organization - FSP services for the Data Management, Biostatistics, Programming, Medical Writing, Lifecycle Safety, and Regulatory Affairs functions - and will ... + 10 years related experience, including 3 years of relevant industry ( CRO /Pharmaceutical) and/or sales experience Req Or + Equivalent combination of education,… more
- Fresenius Medical Center (Columbus, MS)
- …are compiled and submitted in a timely manner to Frenova Renal Research, CRO , study sponsor or IRB as applicable + Assists with maintaining constant communication ... work environment is characteristic of a health care facility with air temperature control and moderate noise levels. May be exposed to infectious and contagious… more