Nicol Brandon MPA,CCRC,CCRP

Experienced Healthcare Professional with over 18 years within the industry and 16 years within the Clinical Research field. I am a strategic thinker that leads by example in tactical executions and is detailed oriented and well organized. Proven ability to manage multiple, complex responsibilities, effectively prioritize tasks, and collaborate with many multi-faceted entities. Areas of significant experience include: Clinical trial planning, execution, and monitoring, certified as a Clinical Research Professional (CCRP) and Certified Clinical Research Coordinator (CCRC) Project management (ACRP-PM) Experience with Phase I, II, III, IV, post-market, and Investigational Device Exemption (IDE) Clinical Trials Working knowledge/application of compliance and regulatory requirements (FDA, IRB, etc.) Clinical project work plans, budget management, and resource planning Experience with identifying key points, integrating data, and assisting with preparing clinical reports, presentations, and publications User acceptance testing and adoption (training), site initiation management Proven ability to lead and motivate teams, work independently, as well as, the ability to work well within a matrix team