Bonnie King, RN, BSN, CMC

Bonnie King, RN, BSN, CMC has over 12 years of experience in the pharmacovigilance field. From 2009 to 2013, they worked as a Senior Product Safety Scientist at Rho, where they were responsible for collecting, monitoring, processing, and distribution of serious adverse events reports within time frames set forth by Sponsors and/or regulatory authorities. From 2010 to 2016, they held positions as a Medical Data Reviewer at UCB Pharma, Case Manager II at Ashfield part of UDG Healthcare plc, and Drug Safety Consultant at Drug Safety Solutions, Inc. In these roles, they were responsible for reviewing SAS and Business Object Reports of Clinical Trial Data, all aspects of post-marketing pharmacovigilance activities, and writing Safety Management plans and designing forms for study start-ups. From 2018 to 2020, they were a Safety Specialist at Catalyst Clinical Research, LLC, a Consultant Nurse (independent contractor) at Venebio Group, LLC, and a Clinical Safety Nurse Consultant at Akebia Therapeutics. In these roles, they provided pharmacovigilance support and case processing duties, performed Quality Assessment of narratives and data entry, and wrote CSR narratives. Currently, they are a Senior Clinical Safety Scientist at HiberCell.

Bonnie King, RN, BSN, CMC has an education history that includes a Bachelor of Science (B.S.) in Nursing Science from Rutgers University - Camden, obtained between 1994 and 1996, as well as a Diploma in Nursing from Helene Fuld School of Nursing, obtained between 1992 and 1994. Additionally, they obtained their Registered Nurse certification from the NC Board of Nursing in June 1997, and their Certified MedDRA Coder certification from MedDRA MSSO in February 2022.