Lisa Beck

Lisa Beck

Director, Clinical Affairs
Background

Ms. Beck is a dedicated, results-driven clinical research professional with over 22 years of experience managing multiple cardiovascular and peripheral clinical research studies for small start-up to multi-national medical device companies.

Prior to joining MCRA, Ms. Beck held leadership positions at the Baim Institute for Clinical Research, formerly known as the Harvard Clinical Research Institute in Boston, MA.

Education

Ms. Beck received her Master of Science in Health Care Administration from the University of Massachusetts, and her Bachelor of Science in Nursing from the University of Vermont.

Experience

Ms. Beck has a proven ability to to build strong partnerships with Sponsors, Clinical Sites, Vendors, and internal team members. Recognized as a skilled leader in executing global cardiovascular clinical research studies, most recently responsible for successfully managing a global IDE study of over 1300 subjects at 90+ sites, resulting in FDA approval.

Over her tenure in clinical research, Ms. Beck has been responsible for managing and/or overseeing more than 40 cardiovascular device studies, many resulting in PMA approval. Within the past 5 years, Ms. Beck has been responsible for leading 5 studies that results in PMA approval in the structural heart, coronary, and peripheral device space.

Overview

At MCRA, Ms. Beck works closely with Sponsors in developing strategies to efficiently operationalize and de-risk clinical research studies in complex subject populations, on time and within budget.

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