Global Regulatory Lead, Gene Editing Programs

Posted yesterday

arbor biotechnologiesSomerville (MA)

Regulatory Affairs Managers Research and Development in Biotechnology (except Nanobiotechnology)

SENIORITY

Manager

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About the role

Arbor Biotechnologies in Cambridge, MA is seeking a Director of Regulatory Affairs to lead global regulatory strategy across our preclinical and early clinical portfolio, reporting to the Chief Medical Officer. You will be the primary regulatory contact with FDA and other health authorities, drive designations, plan submissions, and coordinate CROs, medical writers, and consultants to align with development plans.

Before you apply

Applying takes about a minute. These four things decide how fast it moves after that.

Your profile is current

It's what we read first. Occupations, seniority and locations matter more than a long history.

Two examples you can talk through

Not a portfolio — just two pieces of work where you can explain the decisions and what you'd change.

A number in mind

What you're on now and what would make you move. We negotiate better when we know both.

Your notice period

Employers plan around it, and it's the question that stalls offers most often.

Once you apply, someone reads it and calls you before anything reaches the employer — usually within two working days.