At a Glance
- Tasks: Lead global regulatory strategy for innovative gene editing therapies and manage submissions.
- Company: Editas Medicine, a pioneering company in gene editing.
- Benefits: Competitive salary, health benefits, and opportunities for professional growth.
- Other info: Join a dynamic team dedicated to advancing groundbreaking therapies.
- Why this job: Be at the forefront of gene editing and make a significant impact on healthcare.
- Qualifications: Extensive experience in regulatory affairs and strong leadership skills.
The predicted salary is between 139950 - 171050 $ per year.
Editas Medicine is seeking a Vice President, Regulatory Affairs to lead the global regulatory function for in vivo gene editing therapies.
You will implement strategy, manage submissions, and act as the primary regulatory advisor to executives and partners.
Reporting to the Chief Medical Officer, you will oversee interactions with health authorities, steer evidence-generation plans, and drive regulatory readiness across development programs in a lean organization.
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Head of Regulatory Affairs, Gene Editing employer: Editas Medicine
Editas Medicine is an exceptional employer that fosters a collaborative and innovative work culture, particularly in the vibrant biotech hub of Cambridge. Employees benefit from continuous professional development opportunities, a commitment to regulatory excellence, and the chance to make a meaningful impact in advancing cutting-edge therapies. With a focus on quality systems management, team members are empowered to contribute to significant advancements in healthcare while enjoying a supportive environment that values their expertise.
