Madalena Gryncewicz, MS

Madalena Gryncewicz is a Senior Regulatory Affairs Associate at NMDP with over six years of professional regulatory experience in clinical trials and cellular therapies. She supports INDs, interprets regulations and helps drive process improvements. Her previous role at the Yale Cancer Center involved managing regulatory documentation and IRB submissions for hematologic oncology trials. Madalena holds an MS in Regulatory Affairs with a concentration in Clinical Research from Northeastern University and a BA in Psychological Science from Central Connecticut State University. As a member of RAPS, she values continuous learning and stays up to date with the evolving regulatory landscape.