LMK Clinical Research Consulting
Suzanne N. has extensive experience in clinical research and regulatory affairs, currently serving as a TMF Project Manager at LMK Clinical Research Consulting since 2018. Prior to this role, Suzanne worked as the Assistant Director of Regulatory Affairs at NYC Health and Hospitals Corporation from 2014 to 2017. Additionally, Suzanne has a background as a Clinical Trial Associate at Forest Research Institute, where employment lasted from 2007 to 2013.
LMK Clinical Research Consulting
Inspection Readiness. Two words that can ignite worry, fear, and stress. At LMK, we work with our clients to alleviate those concerns and ensure that you are inspection ready from Day One. We believe that the clinical trial content is the foundation of every clinical trial, and a strong foundation is key to the overall health and stability of any clinical program. LMK takes a proactive approach and makes clinical trial content quality a top priority on an ongoing basis - from start through closeout - not just pending an inspection or trial completion. Don't let your content be a collection burden at the end of a trial! It is a management tool throughout the life of your trial. LMK can help you plan, collect, and maintain your clinical trial content cost effectively without jeopardizing quality. We offer our clients a combination of expertise, tools, processes, and extensive knowledge of the clinical drug development process. Our experts will assess your study requirements and processes and create a plan customized to meet your specific needs. LMK is a division of TransPerfect Life Sciences. TransPerfect Life Sciences provides a full suite of e-clinical, product development, language, and technology solutions to our clients. From idea to launch, we help you every step of the way.