End of Study Data: Best Practices

  1. Whose data is it anyway – site or sponsor? If it’s the site’s data, should all the data be sent to the site?
  2. Best practice for audit trails
  3. Practical considerations for end of study data transfers, archival and closure processes

Booth: #10

Aloft Boston Seaport District, Boston, Massachusetts


Day 1 Tuesday, October 17th @ 2:00-2:45pm EST

October 17, 2023
October 18, 2023


Craig Mooney image

Craig Mooney

Vice President, Scientific E-tech Enabled Services, Calyx

Craig Mooney has nearly 30 years’ experience in the clinical development industry, with concentrated focus on optimizing IRT to improve clinical trial efficiencies. Craig brings a unique understanding of IRT from both a delivery and user perspective, having served as the Director of IRT at Bristol-Myers Squibb for most of the past decade and having held roles in clinical operations, IMP packaging, and labeling & logistics. He is considered an industry expert and has been a featured speaker at numerous IRT conferences including positions as Conference Chairman.

Stay Updated

Never miss a beat. Sign up to receive emails covering industry news and useful content to help you advance clinical development.

  • This field is for validation purposes and should be left unchanged.