I've been proud that my own baby has gotten "my" vaccine! The vaccine went on to be approved in the US and dozens of countries around the world. I was the lead programmer (and later a manager) for the program, where we worked on vaccine trials. Then I worked for a big CRO, dedicated to a single pharma company. I worked first for a very small CRO that focused only on generic drug trials, which was really interesting and fast-paced work. Before this, I worked in the pharma industry as a Statistical Programmer for 8 years. I have been with SAS for a little over 3 years in my current role. There's always something new to learn about CDI, as with all SAS products, but I've seen a lot by now! I have migrated CDI installations from one version to another. I've installed and re-installed CDI on simple, single-box and complex, multiple-server installations. I've created custom data standards and custom compliance checks. I've designed permissions models for CDI installations. I have set up new environments from a Clinical Administrator perspective, importing new standards, setting up controlled terminology packages, defining default content, and setting up the folder structure. I have used it to do "real work" for some of our clients, mapping domains for live clinical studies. I have been using CDI for about three years, and I've done just about every task you can think of with the product. I am Melissa Martinez, Senior Health and Life Sciences Industry Consultant at SAS.
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