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Mintz Levin Makes Changes to Boston and New York Teams


Mintz Levin Makes Changes to Boston and New York Teams

Summary: The Boston and New York offices of Mintz Levin have welcomed new members to their teams from Locke Lord and Epstein Becker & Green.
Mintz Levin Makes Changes to Boston and New York Teams

Law firm Mintz, Levin, Cohn, Ferris, Glovsky and Popeo, P.C. is welcoming new additions to their team. The Real Estate Practice has had Rebecca A. Lee, formerly of Locke Lord LLP, join the Boston team. The New York office has added partner Bethany Hills and associate Benjamin Zegarelli to their Health Law Practice.

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Lee has experience in a broad range of real estate matters where she represents developers, lenders, corporations, and nonprofits in things such as leasing, financing, site acquisitions and assemblages, condominium creation and dispositions, and procuring entitlements. The majority of her focus has been on development permitting and land use in the Boston area. Lee received her J.D. from Yale University, an M.P.A. from Harvard University’s John F. Kennedy School of Government, and a B.A. from Brandeis University.

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Hills is a leader in health law issues such as FDA counseling and guidance, but also has extensive experience working with companies on issues of reimbursement, regulatory, and compliance matters. Managing Member of the New York office Stephen J. Gulotta Jr said, “Bethany brings to the table an extensive knowledge of the health care delivery system which will prove to be invaluable to our clients, especially as the industry continues to evolve. As a time when issues surrounding the FDA approval process are receiving heightened attention, Bethany and Ben’s FDA expertise further strengthens our nationally renowned health law practice and adds greater depth to our capabilities in New York.”

Zegarelli helps clients with federal and state laws that involve manufacturer product development and marketing. This work has included the development of policy positions and submission of comments to the FDA regarding the analysis and drafting of 510(k) applications.

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