- University of Pennsylvania (Philadelphia, PA)
- …CRC will be responsible for the coordination of complex medical dermatology clinical research protocols, including accurate data collection and overseeing the ... quality of the clinical trial data and records, scheduling and conducting study initiation and...and maintain all documentation required by the sponsor or CRO per GCP - includes source documentation, case report… more
- University of Pennsylvania (Philadelphia, PA)
- …performed. He/she will be responsible for supporting the following aspects of clinical trial coordination including subject recruitment, detailed data entry, ... The CRC will assist in the coordination of complex clinical research protocols, including accurate data collection...and maintain all documentation required by the sponsor or CRO per GCP - includes source documentation, case report… more
- Bristol Myers Squibb (Princeton, NJ)
- …and validation partnering with Translational Sciences colleagues when applicable + Manages clinical biomarker data delivery and analysis and associated timelines ... and be responsible for setting strategy for translational activities including clinical biomarker activities to support drug development programs. This individual… more
- ThermoFisher Scientific (Richmond, VA)
- …of issues in consultation with the Global Medical Indication Lead + Interpret the clinical trial data for regulatory documents (eg CSR, INDs, Annual Reports, ... team, in order to provide reliable, high quality study data within time and budget. **A day in the...years of industry experience required. Experience should be in clinical development in a Pharmaceutical, Biotech or CRO… more
- Otsuka America Pharmaceutical Inc. (Annapolis, MD)
- …day-to-day operations of assigned trial(s), as assigned.** **Participates in ongoing review of clinical trial data focusing on data integrity, trending and ... **Job Summary** Under the direction of the Director/Associate Director of Clinical Management, the Senior Clinical Study Manager is responsible for the oversight… more
- BeOne Medicines (San Mateo, CA)
- … questions from sites, IRBs/IECs, Health Authorities, and CROs + Review, query, and analyze clinical trial data + Interpret, and present clinical trial ... selection of investigator and vendors + Train BeiGene colleagues, CRO staff, and study site staff on the therapeutic...data both internally and externally + Represent a clinical study or development program on one or more… more
- BeOne Medicines (San Mateo, CA)
- … questions from sites, IRBs/IECs, Health Authorities, and CROs + Review, query, and analyze clinical trial data + Interpret, and present clinical trial ... selection of investigator and vendors + Train BeiGene colleagues, CRO staff, and study site staff on the therapeutic...data both internally and externally + Represent a clinical study or development program on one or more… more
- BeOne Medicines (San Mateo, CA)
- … questions from sites, IRBs/IECs, Health Authorities, and CROs. + Review, query, and analyze clinical trial data . + Interpret, and present clinical trial ... selection of investigator and vendors. + Train BeiGene colleagues, CRO staff, and study site staff on the therapeutic...data both internally and externally. + Represent a clinical study or development program on one or more… more
- Charles River Laboratories (Mattawan, MI)
- …workplace opportunities. Essential Functions: + Responsible for the interpretation of clinical pathology data and preparation of comprehensive clinical ... pathology reports. Aid Study Directors in the interpretation of clinical pathology endpoints. + Serve as Study Clinical Pathologist or Principal Investigator on… more
- Amgen (Washington, DC)
- … input into safety and regulatory interactions. + Interpret and communicate clinical trial data . + Author/review CSRs, publications, and regulatory submissions ... Join us and transform the lives of patients while transforming your career. Clinical Research Medical Director, Uplizna **What you will do** Let's do this. Let's… more
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