- Takeda Pharmaceuticals (Boston, MA)
- …these activities, and is accountable for the successful design and interpretation of clinical studies . Presents study conclusions to Management and determine ... **Synopsis / Protocol Development, Study Execution, & Study Interpretation** + Drives clinical science activities.../ approval of synopses, protocols and the conduct of clinical studies . Serves as an advisor to… more
- University of Pennsylvania (Philadelphia, PA)
- …Cancer Center at Pennsylvania Hospital's Clinical Research Unit seeks a full-time, Clinical Research Nurse (CRN) to conduct studies involving a wide variety ... sponsors. This position will report directly to the Research Manager and work directly with Physician Investigators ("PI") on clinical research performed.… more
- University of Pennsylvania (Philadelphia, PA)
- …the DOM Clinical Trials Unit supports a diverse group of investigators, involving work on a wide spectrum of clinical trials ranging from phase I to ... industry initiated, different disease states and varying complexities. Research coordinator work includes study design, protocol development, submission to… more
- University of Rochester (Rochester, NY)
- …Assists in the planning, coordinating, implementing, monitoring, and evaluating specific clinical research studies as assigned. Assists in day-to-day operations ... and the implementation of clinical research protocols. Assists in carrying out ...in protocol-related training as required. + Complies with Good Clinical Practice and the Code of Federal … more
- Texas Health Resources (Dallas, TX)
- …30 days of hire and maintained every 2 years What You Will Do * Conduct clinical studies according to FDA, CFR and ICH regulations and guidelines: from pre- ... positive manner * Develop and implement recruitment strategies for studies ; which include screening potential study subjects...records of the receipt, administration, and return of all clinical supplies (including study drug). Assist in… more
- UTMB Health (Galveston, TX)
- …with the Scientific Director for the Institutional Office of Regulated Nonclinical Studies (ORNcS), study sponsors and/or funding agencies to design and ... Responsible for the overall planning, conduct and reporting of non- clinical regulated studies , in accordance with applicable...projects. + Supervise a scientific team to conduct regulated studies and ensure the study is performed… more
- CSL Behring (King Of Prussia, PA)
- …with Senior Managers, Clinical Finance to build and maintain robust study costing models for studies within remit, ensuring clarity around assumptions ... and dynamism within model. + Work in partnership with Clinical Operations and POE to ensure study assumptions for all studies are up-to-date and reflect… more
- University of Pennsylvania (Philadelphia, PA)
- …limited to screening and enrollment of participants, collection and entry of clinical , imaging and anthropomorphic data, coordination of study activities across ... assisting with Institutional Review Board (IRB) submissions and inquiries. The candidate will work closely with the Principal Investigator and study team to… more
- IQVIA (Norwich, CT)
- **Job Title:** Clinical Trial Nurse - Norwich, CT ** Work Set-Up:** Onsite support. **Scheduled Weekly Hours:** 34 hours **Job Overview:** Coordinate and ... participate in clinical research studies ensuring that ...are carried out according to protocol, contracted scope of work , good clinical practice, sponsor standard operating… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …these activities, and is accountable for the successful design and interpretation of clinical studies . Presents study conclusions to Management and determine ... **Synopsis / Protocol Development, Study Execution, & Study Interpretation** + Drives clinical science activities.../ approval of synopses, protocols and the conduct of clinical studies . Serves as an advisor to… more