Janice del Rosario

Director Of Trial Master File Services | Clinical Operations at LMK Clinical Research Consulting

Janice del Rosario has extensive work experience in the clinical research consulting and operations field. Janice worked at LMK Clinical Research Consulting from 2019 to the present, starting as a TMF Consultant and later becoming an Associate Director of Clinical Operations. Currently, they hold the position of Director of TMF Services | Clinical Operations.

Prior to their role at LMK Clinical Research Consulting, Janice worked at Parexel from 2005 to 2019. Their roles at Parexel included TMF Business Process Lead, Strategic Partnerships, Manager of Clinical Operations & Records Management, Associate Manager of Clinical Operations, and Clinical Research Assistant.

Janice's career in the industry began at the University of California San Diego in 2000, where they worked as a Research Assistant and later became a Research Psychometrist.

Their strong background in various roles within clinical research consulting and operations makes their a valuable asset in the field.

Janice del Rosario has earned a Bachelor's degree in Psychology from UCLA. No specific start or end year for their education at UCLA is provided.

Location

San Diego, United States

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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.