Responsibilities : Hands-on SAS Programming for creation and QC of clinical Tables, Listings and Graphs. Perform validation and QC of the programs, datasets and statistical reports per study requirements. Authors SDTM and Adam dataset specifications including the identification of potential data issues or areas of critical data examination. Deliver end-to-end programming of deliverables from CRF design through Electronic Submissions (ESUB) components. Other related programming activities. Requirements : 5+ years of Statistical Programming experience within the life science industry, preferably on the Sponsor side and relevant BS degree Submissions experience, preferably BLA/NDA. Experience in Ophthalmology is a plus*. Expertise with SAS statistical software. R programming is a plus*. Experience supporting regulatory submissions and submissions requirements, relevant ICH and FDA/EMEA/ROW guidelines. Experience and understanding of drug development process and clinical trial. Katalyst Healthcares and Life Sciences
...marketing agency in Newmarket, NH is seeking a Production Associate to assist with various production tasks including Heat Press and Screen Printing. This is a training-level position suitable for anyone looking to grow in the industry. Candidates should exhibit reliability,...
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...but there are a few requirements that help us determine whether someone will have the skill set to be able to learn quickly. Cabinet Maker We are looking for someone who has experience in cabinetry or carpentry. We work with all sorts of cabinet materials: plywood...
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...Description Job Summary As a CBRE, GDS Commercial Cleaner, you will be responsible for basic cleaning duties. This includes mopping, sweeping and trash disposal. You will be responsible for ensuring the cleanliness of your assigned areas. Primary Job Functions...