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Scribe Therapeutics is a molecular engineering company focused on creating best-in-class in vivo therapies that permanently treat the underlying cause of disease. Founded by CRISPR inventors and leading molecular engineers Benjamin Oakes, Brett Staahl, David Savage, and Jennifer Doudna, Scribe is overcoming the limitations of current genome editing technologies by developing custom engineered enzymes and delivery modalities as part of a proprietary, evergreen CRISPR by Design™ platform for CRISPR-based genetic medicine.
We are seeking a highly creative, passionate, and motivated individual to join us in our quest to develop the next generation of CRISPR-based therapeutics. The current role is for a Senior Director, Regulatory Affairs to join our team and advance our platform. The candidate should have a passion for working collaboratively with nonclinical, clinical and CMC team members to enable building regulatory strategies for CRISPR-based therapeutics. Furthermore, the candidate would offer expertise in efficiently navigating the regulatory complexities inherent in gene editing programs.
Key Responsibilities:
Salary will be commensurate with experience. We will provide an intellectually stimulating, collegial and fast-paced environment. If you are ready to engineer the future of therapeutics, then we are excited to hear from you! Visit us at www.scribetx.com.
We are committed to creating a diverse environment and are proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, disability, age, or veteran status.
At the time of posting, the base pay wage range for this role is $230,000-285,000 per year. The offered pay range will depend on internal equity and the candidate’s relevant skills, experience, qualifications, training, and market data. Additional incentives are provided as part of the complete package in addition to comprehensive medical and other benefits.
Full Time
$187k-255k (estimate)
03/14/2024
07/09/2024
scribetx.com
Alameda, CA
<25
The job skills required for Sr. Director, Regulatory Affairs include Regulatory Affairs, Leadership, Regulatory Compliance, Alignment, Drug Development, etc. Having related job skills and expertise will give you an advantage when applying to be a Sr. Director, Regulatory Affairs. That makes you unique and can impact how much salary you can get paid. Below are job openings related to skills required by Sr. Director, Regulatory Affairs. Select any job title you are interested in and start to search job requirements.