LMK Clinical Research Consulting
Kristen Gunther is an experienced project manager currently employed at LMK Clinical Research Consulting since December 2022. Prior to this role, Kristen held various positions in clinical research, including TMF Study Owner for Clinical Trials at ExecuPharm from May 2017 to May 2021 and Clinical Trial Manager at both PPD and Exelixis from November 2010 to May 2017. Earlier in Kristen's career, roles included Clinical Trial Associate at ExecuPharm and BLCPro, as well as positions in technical consulting and logistics coordination. Kristen earned a Bachelor's degree in Communication from Central Connecticut State University between 2000 and 2003.
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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.