- Regeneron Pharmaceuticals (Sleepy Hollow, NY)
- …study team meetings, data oversight review sessions, and works closely with CRO medical monitors in support of medical affairs clinical trials. * Oversees and ... provides hands on support in management , generation and dissemination of clinical and non-clinical data that supports the medical strategy and results in high… more
- Takeda Pharmaceuticals (Boston, MA)
- …them. + Responsible for high impact global decisions: monitoring and interpreting data from ongoing internal and external studies, assessing the medical and ... in these activities, and be accountable to senior company management for the successful completion of underlying objectives. For...necessary to ensure achievement of related goals. + Interprets data from an overall scientific standpoint as well as… more
- HistoWiz (Long Island City, NY)
- …process tissue specimens and digitize all of the results, hosting our client's data on a proprietary platform, PathologyMapTM . This platform not only enables ... individually. This online platform also contains the world's largest collection of pathology data and the first network of top pathologists. Today, we are expanding… more
- University of Miami (Miami, FL)
- …audits, reviewing consolidated records (the results of the records once the new data are added), designing, reviewing and testing the revised treatment matrix which ... will identify possible cancers from claims data . The RA1 will facilitate the process of preparing required regulatory documentation for initial and subsequent study… more
- BeOne Medicines (Emeryville, CA)
- …and provides regular updates on study progress in the region to senior management and Global Clinical Study Manager as required + Represents the regional study ... expertise **Timelines, Planning and Execution** + Leads planning and management of the assigned clinical study(ies) from feasibility through...study for countries in region + Manages the trial data collection process for the region, drives data… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …Recommends high impact global decisions. + Responsible for monitoring and interpreting data from ongoing internal and external studies, assessing the medical and ... accountable for the successful design and interpretation of clinical studies. + Interprets data from an overall scientific standpoint as well as within the context… more
- Charles River Laboratories (Northridge, CA)
- …industry regulations and standards. This position will also oversee the management of regulatory documentation related to the organization's Institutional Review ... qualification of suppliers performing collections. The position works closely with QA management staff, the Medical Director, Operations Team, etc. to ensure all… more
- Charles River Laboratories (Mattawan, MI)
- …single operational area with oversight + Execute review and approval of data with oversight for final scientific/technical decisions within a single operational area ... limited complexity/scope in one operational area with minimal oversight + Perform data analysis using appropriate software with minimal oversight + Develop critical… more
- Eurofins (Auburn, ME)
- …meet the technical quality objectives required by various accrediting bodies. + Assists with data entry, quality control , and sample receipt as needed. + Develop ... food, environment and pharmaceutical products testing and in agroscience CRO services. It is also one of the global...a compliant manner which allows it to produce defensible data . + Prioritizes the activities of the operations groups… more
- Sanofi Group (Morristown, NJ)
- …the validation gap(s) on the selected COA instruments (including vendor management ) + Prepare the scientific documents (reports, regulatory documents, publications, ... ideally expected (indicative):** + Relevant experience in COA in Pharma/ CRO /Consultancy: ideally proven track record from scientific publications in core… more