Jessica Mccoy

Biography

 Jessica McCoy joined MedSource in July 2016 and is the Manager of the Study Start-Up & Regulatory Affairs Department. She is based out of our Raleigh office location and leads the feasibility, site identification, trial master file, and site start-up/activation teams. In addition to participating in the strategic development and planning of overall clinical operations, Jessica assists with the general management of the Raleigh office. She has over 10 years of experience in management of study start-up and regulatory affairs for Phase I-IV global clinical research trials within the CRO industry. Jessica has extensive experience in hematology/oncology and central nervous system studies as well as other various complex disease indications. Prior to joining MedSource, Jessica worked at various Clinical Research Organizations where she played a key role in strategy and timeline development of global clinical trials. This included but was not limited to proposal progression, study start-up implementation, facilitation of ethics committee and regulatory submissions, contract negotiations, delivery of study milestones, and overall project execution. Jessica also has several years of experience in training and mentoring project team members. She began her career in clinical research as a Study Coordinator after finishing her undergraduate degree at Miami University of Ohio.

Research Interest

 Cancer