- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- …for internal and external studies + Oversees and provides input to the study drug and clinical supplies forecasting, drug accountability and drug ... (SOPs) and ICH/GCP. This role applies to internally sourced studies and studies out-sourced to Clinical Research...database lock, reconciliation of vendor contracts, budget, TMF, and study drug accountability + Contributes to clinical… more
- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- …for internal and external studies + Oversees and provides input to the study drug and clinical supplies forecasting, drug accountability and drug ... (SOPs) and ICH/GCP. This role applies to internally sourced studies and studies out-sourced to Clinical Research...database lock, reconciliation of vendor contracts, budget, TMF, and study drug accountability + Contributes to clinical… more
- Charles River Laboratories (Reno, NV)
- …in conjunction with other departments to coordinate assignments to facilitate scheduling of study -related processes on assigned studies to ensure protocol or ... in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will...feel passionate about. **Job Summary** We are seeking a Study Coordinator for our Safety Assessment site located in… more
- AbbVie (North Chicago, IL)
- …Toxicology. This role designs, conducts and reports non-GLP and GLP general toxicology studies in support of drug submissions to regulatory agencies, and ... responsibility of this job is to function as GLP Study Director/ Study Director Manager for AbbVie internally...Study Director Manager for AbbVie internally conducted toxicology studies (80% of time) and external sponsor monitor for… more
- BeOne Medicines (Emeryville, CA)
- … study TMF QC plan + Collaborates closely with Global Clinical Supplies to forecast study drug and timely delivery of supplies to sites + Supports and as ... for key resources. + Monitors resource utilization over the study life cycle + Ensures clinical studies at a project level are executed within endorsed time,… more
- GE Vernova (Oakbrook Terrace, IL)
- …+ Load Flow / Power Flow, Reactive Capability and Reactive Compensation, Power Factor Study + Dynamic Performance Studies (DPS) and other design studies ... Voltage Ride Through (LVRT), High Voltage Ride Through (HVRT) study + Arc Flash + Protection studies ...Annual **Healthcare benefits include medical, dental, vision, and prescription drug coverage; access to a Health Coach, a 24/7… more
- BeOne Medicines (San Mateo, CA)
- **Position Summary:** + Accountable for regional study delivery with appropriate inspection readiness quality, within agreed timelines and budget + Acts as regional ... lead for multiple studies across an indication or across a program as...resolution of issues within the region for the assigned study + Ensures alignment of regional deliverables with overall… more
- University of Utah (Salt Lake City, UT)
- …Investigator(s) under supervision of the Research Manager in determining and accomplishing study objectives; oversees research studies in an administrative and ... and/or other regulatory documents and research correspondence. 3. Coordinates participant study visits and related facility, drug /device, and equipment… more
- Caris Life Sciences (Phoenix, AZ)
- …Summary** The Clinical Study Documentation Specialist provides clinical study support for Caris-sponsored studies and collaborative pharmaceutical research ... regulatory requirements, and industry best practices. Responsibilities include maintaining study documentation, coordinating Institutional Review Board (IRB) submissions, engaging… more
- University of Utah (Salt Lake City, UT)
- Details **Open Date** 06/30/2025 **Requisition Number** PRN42341B **Job Title** PS Study Coordinator **Working Title** PS Study Coordinator **Job Grade** D ... the University of Utah School of Medicine has an immediate opening for a Study Coordinator. Working under the direction of the Associate Director for Research, the … more