Terry Smolenski

Terry Smolenski has extensive experience in regulatory affairs and compliance within the clinical research industry. They have held various director-level positions overseeing regulatory documents, study conduct, training, auditing, and compliance with federal regulations and Good Clinical Practice guidelines. Prior to this, Terry has also worked in roles such as Clinical Trial Associate and Research Assistant, gaining experience in data entry, specimen processing, and IRB submissions. In addition, they have managed office operations as an Office Manager.