Clinical Protocol and Data Management

The Clinical Protocol and Data Management (CPDM) is a centralized office composed of trained regulatory, financial, clinical, study management, and compliance personnel who promote uniformity and consistency in clinical research by providing support for principal investigators and patients.

We work closely with patients, physicians, hospital staff, the Protocol Review and Monitoring Committee (PRMC), the Data and Safety Monitoring Committee (DSMC), and the Institutional Review Board (IRB), to ensure clinical trials are run safely and effectively.

CPDM Leadership

• Medical Director: Andrew Lassman, MS, MD, FAAN
• Director, Clinical Research Operations: Frances Brogan MSN, RN, OCN, CCRP
• Assistant Director, Clinical Research Operations: Ryan Shelton, BS
• Assistant Director, Clinical Research Nursing and Quality: Edward Bentlyewski, MSN, APN, NP-C, AOCNP, CCRP
• Finance Managers: Jashira Rodriguez, BS, & Marina Greenberg, MS
• Research Manager, Quality and Safety: Mariangela Agovino, MPH
• Senior Regulatory Manager: Suzanne Mistretta, MS, CCRP
• Regulatory Science Manager: Adam Scott, BS, CCRP

Clinical Research Managers

• BMT/Hematologic Malignancies/Myeloma: Deeksha Kaura, BDS, MS, ACRP-CP
• Hematologic Malignancies/Lymphoma: Beatriz Raposo-Corradini, MSc
• Breast/Cooperative Groups:  Erik Harden, MA
• GU/Urology: Jillian Gray, BS
• Phase I: Alyssa Schumpp, MS
• Melanoma/Sarcoma/Thoracic: Moury Minhaz, MS
• Multi-Center Trials: Naomi Sender, BS,  & Sarah StaAna, MS
• Neurologic Malignancies/GI: Kriti Bagri Manjrekar, MDS, PGD- HP