- Regeneron Pharmaceuticals (Tarrytown, NY)
- … data inputs. + Performs the accessioning and receipt of non- clinical / clinical samples by assessing and verifying data , both manually and with automated ... and written communication with internal and/or external stakeholders to facilitate data discrepancy resolution. Communicates with CRO 's and third-party vendors… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …with some supervision. This position also guides contract research organization ( CRO ) programmers and statisticians in preparing analysis files and performing ... Statistical Analysis Plan (SAP), Statistical Analysis, Results Interpretation, and clinical study report (CSR): Leads statistical activities for complex studies… more
- Charles River Laboratories (Shrewsbury, MA)
- …that you can feel passionate about. **Job Summary** Responsible for reviewing all study data to ensure it is complete and GLP compliant. Ensure that all data ... review follows SOP and regulatory guidelines that apply to the recording of study data . Interact with Scientist, QA staff and other departments with regards to … more
- Eurofins (Rensselaer, NY)
- …leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders ... CDMO, advanced material sciences and in the support of clinical studies. If you're looking for a rewarding career,...liaison to cross functional teams while performing and coordinating data review and data management assignments of… more
- BeOne Medicines (Emeryville, CA)
- …Excel, PowerPoint, Teams and Outlook + Familiar with industry CTMS and data management systems **Other Qualifications:** + Understands clinical trial processes ... quality of trip report, action item management, query management, data currency and TMF management + Responsible for managing...and TMF management + Responsible for managing relationship with CRO FSP line manager and liaising to understand and… more
- Norstella (Columbia, SC)
- …**About Citeline:** Citeline is one of the world's leading providers of data and intelligence on clinical trials, drug treatments, medical devices ... Clinical Solutions combining platform, services and Real World Data (RWD) offerings to support use cases across the...activities **Qualifications:** * 5+ years experience in working in clinical trial relevant business either CRO , trial… more
- Eurofins (Rensselaer, NY)
- …leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders ... discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies. If you're looking for a rewarding career, apply with us… more
- Amgen (Washington, DC)
- …Data File (SDF) specifications, other key-study related documentation, protocol deviations, Data Quality Review (DQR), Flash Memos, Clinical Study Reports ... **Responsibilities** + Provides statistical contributions, statistical review and quality control of Study Concept Documents (SCDs), protocols, randomization specifications,… more
- University of Pennsylvania (Philadelphia, PA)
- …Title Substance Use Navigator (Department of Emergency Medicine) Job Profile Title Clinical Research Coordinator B Job Description Summary This full-time, in person ... organize and maintain all documentation required by sponsor or CRO (case report forms, source documentation, study and regulatory...binders) + Assist in the coordination of Phase I-IV clinical trials + Participate in the conduct of study… more
- ICON Clinical Research (New York, NY)
- …information as required to other departments within ICON Laboratories (and ICON Clinical CRO if appropriate). + Enter protocol parameter information into ... study specific inquiries from Sponsors, Physicians, CRA and CRO representatives and the ICON Site Services Department. +...area serving clinical trials, such as IVRS, Clinical Supplies Packaging and Distribution, Medical Imaging, Data… more