- Regeneron Pharmaceuticals (Tarrytown, NY)
- …educational materials, trainings) + In collaboration with Clinical Study Team (CST), completes clinical data reviews and activities prior to data cuts as ... The Study Medical Director, Clinical Sciences is responsible for facilitating assigned ovarian...interim analyses, DBLs, regulatory submissions, etc.) + Communicates with CRO and study site personnel including investigators to answer/triage… more
- Gilead Sciences, Inc. (Foster City, CA)
- …SOPs, company policies and regulatory guidelines to provide timely and high-quality clinical data that supports global registration and commercialization of ... Gilead and help create possible, together. **Job Description** **POSITION OVERVIEW:** Clinical Operations is responsible for the worldwide execution of all Phase… more
- BeOne Medicines (San Mateo, CA)
- …from sites, IRBs/IECs, Health Authorities, and CRO 's + Review, query, and analyze clinical trial data . + Interpret, and present clinical trial data ... The Director, Clinical Development will support BeOne Clinical ...selection of investigator and vendors. + Train BeOne colleagues, CRO staff, and study site staff on the therapeutic… 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 ... of the Global Research organization in BMS and leads late stage clinical , pharmacological and translational research and development activities for the pipeline and… more
- BeOne Medicines (Emeryville, 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 BeOne 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
- ThermoFisher Scientific (Alachua, FL)
- …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
- Charles River Laboratories (Mattawan, MI)
- …collaborations and training. 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
- 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
- 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
- Amgen (Washington, DC)
- … clinical input into safety and regulatory interactions. + Interpret and communicate clinical trial data . + Lead authoring and review of CSRs, publications ... Join us and transform the lives of patients while transforming your career. ** Clinical Research Medical Sr. Director - Thoracic Oncology** **What you will do** Let's… more
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