Job Description Prepares scientific and regulatory documents on behalf of government and private sector clients for submission to the Food and Drug Administration (FDA) (Investigational New Drug applications, annual reports, preclinical and clinical study reports, safety reports, and investigator's brochures). Performs literature searches and/or prepares summaries of results. Prepares meeting reports and proceedings, safety documents or data analysis. Contributes to technical proposals and responds to technical questions. Job Requirements Superior writing skills that require moderate to minimal editing. Knowledge of regulatory requirements for clinical studies. Performs core tasks with moderate to minimal supervision. Strong software skills to include Microsoft Office products and reference management software. Excellent time management and multi-tasking skills. Ability to analyze medical research data and review experimental protocols. Meets expectations with regards to work product. This is a hybrid position with 2 days in TRI's Bethesda, Maryland office, and 3 days working remotely. #J-18808-Ljbffr
POSITION IDENTIFICATION Job Title: Intermediate Interior Designer Business Unit: iDNA Reports To: Senior Interior Designer Location: DTLA (On-Site) Start Date: IMMEDIATELY ***ONLY LOCAL CANDIDATES WILL BE CONSIDERED*** COMPANY DESCRIPTION Impact Housing (IH) is a vertically...
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...De Novo, a boutique staffing and recruitment agency is currently seeking document review project attorneys for a 3 month project. Attorneys will be working with a personal injury firm based in Missouri. The project involves reviewing claimant forms for sexual abuse cases...