- Butterball (Garner, NC)
- …industry. Some experience related to the design and execution of challenge studies , validation studies , etc.. Excellent written and verbal communication, ... by law. This position is deemed Safety Sensitive for purposes of Butterball's Drug /Alcohol Screening & Testing Policy. Details will be provided to individuals who… more
- Butterball (Raeford, NC)
- …sanitation, environmental conditions, equipment, and testing methodologies.7. Evaluates and studies laboratory data to generate reports, graphs, and charts for ... by law. This position is deemed Safety Sensitive for purposes of Butterball's Drug /Alcohol Screening & Testing Policy. Details will be provided to individuals who… more
- J&J Family of Companies (Spring House, PA)
- …development of clinical contributions to internal documents and presentations for assigned studies ; including clinical study reports (CSRs) and clinical portions ... of the way. Johnson & Johnson is recruiting for an Associate Director, Study Responsible Physician (SRP) Immunology Translational Sciences and Medicine (TSM) to be… more
- Charles River Laboratories (Spencerville, OH)
- …site located in **Spencerville, OH** . **Basic Summary:** Responsible for overseeing study conduct of preclinical efficacy and/or toxicology studies assigned by ... and ensures regulatory requirements/expectations are met for the assigned study (ies). Overall interpretation of preclinical toxicity studies , evaluation… 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
- 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 for AbbVie internally conducted toxicology studies... Study Director for AbbVie internally conducted toxicology studies (80% of time) and external sponsor monitor for… more
- Taiho Oncology (Princeton, NJ)
- …Objectives: + Coordinates cross functional study team meetings and supports study manager with meeting minutes for assigned studies . + Updates internal ... Study Associate I, Clinical Operations Princeton, NJ, USA...review of the TMF plans to ensure consistency across studies and alignment with internal TMF procedures. + Monitors… more
- Stryker (Memphis, TN)
- …Supports management of clinical data and regulatory reports, and timely management of study publications. + Ensure studies are conducted in compliance with GCP, ... Stryker is hiring an **Associate Clinical Study Manager** to support our **Trauma & Extremities...planning, execution, and oversight of one or more clinical studies . As an integral part of the Clinical Research… more
- BeOne Medicines (Emeryville, 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
- Battelle Memorial Institute (West Jefferson, OH)
- …+ Demonstrated organizational skills and ability to simultaneously work on multiple studies for multiple study directors; + Excellent team-building and ... to apply. **Job Summary** Battelle is currently seeking a ** Study Facilitator** in the High Containment Chemistry division. This...of Good Laboratory Practices (GLP) in support of non-clinical studies ; + Must be a US Citizen to perform… more
