BonaFide Staffing i s looking for an Regulatory Medical Writer/Public Disclosure Home office, 1 day in the office in Central Jersey to be with the team!! Responsible for the preparation/maintenance of Clinical Registry Submission Documents for protocol registration and results disclosure and review for accuracy, spelling and grammatical correctness. Circulate draft document to the study team and incorporate their comments, submitting documents to appropriate Clinical Registry member. Requirements BonaFide Staffing seeks: Regulatory Medical writer with Clinical Registry experience. MS or PhD in Life Sciences with at least 3 years experience in writing of Protocols, Clinical Study Reports and Informed consent Forms. Background in preparing Protocol Registration and results disclosure for international registries including clinicaltrial.gov preferred and ability to clearly write medical lay-language documents. Identify and work with study-responsible clinical staff and provide guidance around clinical registry processes. Must have experience working in Pharmacological and with Clinical Registry. Relocation not available at this time, looking for NJ/NY/PA candidates that can travel on-site to NJ... Thank you