November AGRE Webinar

3rd Nov, 4:00 pm, Eastern time, USA

3rd Nov, 9:00 pm, Europe

3rd Nov, 12:00 midnight, Middle East

4th Nov, 7:00 am, Sydney, Australia 

Zoom Link: https://uni-sydney.zoom.us/j/83264708282?from=addon

Presenters:

Monique Carter is a Regulatory Scientist. She is currently a Senior Director and Global Lead at Pfizer in Global Regulatory Affairs – Global Product Development in Internal Medicine. At Pfizer, Monique leads innovative and adaptive

drug development strategies ranging from the early investigational space through post marketing approval. Prior to joining Pfizer, Monique worked as a cross-functional regulatory and clinical development strategy team leader across the drug development continuum spanning a host of therapeutic areas in global biotechnology investment firm and management consulting settings.

Monique is an appointed member of the RAPS Regulatory Focus Editorial Advisory Committee. She holds a BA in Biochemistry and Physics from Baylor University and a MS in Biotechnology with a concentration in Regulatory Science from Johns Hopkins University. She has been recognized as a global leader in regulatory affairs by her RAPS

recognition as a Fellow.

Jessica Fritter received her Bachelor’s in Communication Studies from the University of North Carolina Wilmington and obtained her Master of Applied Clinical and Preclinical Research from The Ohio State University. She is currently completing her Doctor of Health Sciences at Eastern Virginia Medical School. She has her Association of Clinical Research Professionals (ACRP) - Certified Professional Certification. Jessica is on the Faculty at The Ohio State University, Master of Clinical Research program where she teaches and creates courses on clinical research. She has managed multimillion dollar infrastructures and clinical trial budgets along with overseeing a core infrastructure of regulatory affairs, clinical research training, compliance, business operations, clinical trial management systems, feasibility, and program management. She has extensive experience in study feasibility, creating training programs, writing grants, grants management, study start up through close out for federal RCTs, industry sponsored trials, and internal collaborative studies.