Please Wait...

Ronald Van Heertum

Translation skills

Main profile

Ronald Van Heertum, MD
Vice President of Molecular Imaging

Dr. Van Heertum is responsible for the management and implementation of all aspects of Molecular Imaging. Prior to coming to BioClinica, Dr. Van Heertum was Professor and Executive Vice Chairman/CAO, Department of Radiology at Columbia University College of Physicians & Surgeons as well as Director of Nuclear Medicine and PET. In this position he participated in many clinical trials in oncology, neurology, and psychiatry and established an international reputation in SPECT and PET imaging. He has authored or co-authored over 200 publications and is the editor of a book on Brain Imaging that is now in its 4th Edition. He has been an active member of the RSNA, American College of Radiology where he is an FACR and the Society of Nuclear Medicine.

Authored Publications

Van Heertum RL, Scarimbolo R, Wolodzko JG, Klencke B, Messmann R, Tunc F, Sokol L, Agarwal R, Strafaci JA, O'Neal M.  Lugano 2014 criteria for assessing FDG-PET/CT in lymphoma: an operational approach for clinical trials.  Dovepress.  13 June 2017 Volume 2017:11 Pages 1719—1728.

Van Heertum RL, Scarimbolo R, Ford R, Berdougo E, O’Neal M. Companion diagnostics and molecular imaging-enhanced approaches for oncology clinical trials. Drug Design, Development and Therapy 2015:9 5215–5223.

LEARN MORE OR SPEAK WITH OUR EXPERTS

CONTACT US
Leader in Clinical Trial
Management Solutions

Successful clinical trials require the ability to see key details and uncover hidden insights. Bioclinica utilizes science and technology to bring clarity to clinical trials, helping companies to develop new life-improving therapies more efficiently and safely.

Don't compromise with manual systems and spreadsheets. As an entry-level system with phased implementation, Bioclin… https://t.co/0EfLrNpuxJ
Bioclinica (Yesterday)
Bioclinica #EDC Solo delivery model offers the full features and functionality of Bioclinica EDC with the freedom a… https://t.co/zBylq6LqyR
Bioclinica (2 days ago)
Think a #CTMS implementation takes too much time and too many resources? It doesn’t have to. Learn how a configurab… https://t.co/yowxvVTyP3
Bioclinica (2 weeks ago)
We think you should have access to the full suite of #ClinicalDataManagement services to ensure high-quality, relia… https://t.co/jVuliQwFo3
Bioclinica (3 weeks ago)
A mid-study change to a new #IRT vendor can be required for a number of reasons and can introduce a certain amount… https://t.co/sU7akWjdCD
Bioclinica (3 weeks ago)
A clinical trial rescue or transition presents a unique set of challenges for study teams. Join us on July 21 for a… https://t.co/rlYiFYpR6G
Bioclinica (4 weeks ago)