Summary
Connie Clark is a Quality Assurance Specialist with over a decade of experience and five years leading GLP program development at the US Army Medical Research Institute of Chemical Defense. She combines deep regulatory knowledge of 21 CFR 58 and 21 CFR 11 with hands-on skills in SOP writing, audit management, and computer/software validation to ensure research compliance with FDA, MRMC, and Army standards. Connie has a strong operational background from managing a Cholinesterase Analysis laboratory, where she developed analytical methods, maintained complex instrumentation, and trained personnel under chemical surety conditions. She excels at translating audit findings into targeted training modules and practical corrective actions, and she routinely interfaces with external regulatory stakeholders to keep practices current. Based in Maryland with a BA in History, Connie brings a rare blend of laboratory technical expertise, meticulous documentation practices, and instructional design that improves both quality and investigator proficiency.
11 years of coding experience
BA, History, BA, History at Towson University