Peggy Zorn, MS, MBA

Associate Director, Regulatory Affairs, Submissions, and Transparency

Ms. Peggy Zorn is the Associate Director of Regulatory Affairs, Submissions, and Transparency with over 20 years of experience in regulatory affairs, drug safety, scientific information resources and IT. She is responsible for the management and oversight of all regulatory writing, operations and submission activities, including the preparation, publishing, and QC, and electronic submission of regulatory submission documents following eCTD guidelines. Previously, Ms. Zorn was a Regulatory Submissions Lead and Associate Director of Worldwide Regulatory Affairs at Pfizer. Ms. Zorn holds a Masters in Business Administration degree from Madonna University and a Masters of Science degree in Library Science from Wayne State University. She also earned a Regulatory Affairs Essentials Certificate from the University of California

Joe Archer

Associate Director, Trial Disclosure Services

Mr. Joe Archer is the Associate Director, Trial Disclosure Services, and instrumental in the launch and growth of the clinical trial disclosure business at MMS. Mr. Archer has over 20 years of experience in clinical research and is a Subject Matter Expert of processes and systems related to the reporting of clinical trial information to ClinicalTrials.gov. Prior to holding this role, Mr. Archer was Senior Manager, Clinical Trial Disclosures at GlaxoSmithKline from 2007 to 2011 where he led the development and oversight of systems, processes, quality controls and compliance of clinical disclosure reporting of the company’s protocol and results summary information. He has also held various positions of increasing responsibility in the Regulatory Quality Control and Strategic Operations divisions of INC Research, Pfizer, and Parke-Davis. Mr. Archer earned a Bachelor of Science degree in Health Care Administration from Eastern Michigan University.

Zach Weingarden, MSE

Zach Weingarden is a Technical Project Manager with over eight years of experience in the healthcare and CRO arena.  Mr. Weingarden has managed software implementations including TrialAssure™  as well as EMR systems in fast-paced and demanding healthcare, research, biotech and pharma environments.  Adept at analyzing business workflows and aids in the design, configure and testing of  TrialAssure™ software that aligns with organizational needs and objectives.  Demonstrated ability to manage application developers, technical services representatives, and client analyst teams to ensure projects met strict deadlines and adhere to budget constraints.  Mr. Weingarden holds a Master of Science in Biomedical Engineering concentrating in Biotechnology and a Bachelor of Science in Industrial and Operations Engineering.