Job Overview Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. Essential Functions Assist Clinical Research Associates (CRAs) and Regulatory
Responsibilities: Annotate Case Report Form (acrf.pdf) following FDA/CDISC or sponsor guidelines. Develop SDTM specifications and generate SDTM datasets using SAS. Develop ADaM specifications and generate ADaM datasets using SAS based on Statistical Analysis Plan. Develop Tables,
Job Overview Serve as the liaison between Records Management and user departments regarding Trial Master files. Apply clinical research Records Management expertise to provide project related assistance across multiple project(s), sites, and project teams. Ensure all work
Responsibilities: Annotate Case Report Form (acrf.pdf) following FDA/CDISC or sponsor guidelines. Develop SDTM specifications and generate SDTM datasets using SAS; Develop ADaM,specifications and generate ADaM datasets using SAS based on Statistical Analysis Plan; Develop Tables, Listings,
Duties & Resposibilities Develop and evaluate packaging materials based on quality, functionality, cost, and product requirements. Conduct packaging testing and trials & coordinate with Product Development. Source and evaluate packaging and printing suppliers. Coordinate supplier samples, prototypes, quotations,
Grow Beyond UR Job with URC Universal Robina Corporation is looking for a Scientist Packaging Scientist PD Scientist (Confectionery) PD Scientist (Snacks) PD Scientist (Bakery) PD Scientist (Bev/RTD) The Scientist will work on materials and/or processes
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