Lisa McAllister

Lisa McAllister has worked in various positions related to clinical trial documentation and regulatory records, starting as a Document Control Specialist and gradually advancing to their current role as a Records Associate II at Just in Time GCP. Lisa has experience in performing quality checks, managing electronic trial master files, and ensuring compliance with client business rules and SOPs. Lisa has also served in roles such as Clinical Trial Administrator, eTMF Specialist, and Office Manager, showcasing their expertise in document management and record-keeping within the healthcare and pharmaceutical industry.