Join us and be a part of that transformation.
To support its growth and expansion, Fractyl is seeking a Senior Regulatory Affairs Specialist, reporting to the Director of Regulatory Affairs. This role involves participating in the day to day operations of the department as it relates to supporting business needs. This individual will assist in writing and submitting various regulatory submissions and reports, providing guidance to new product development, and help enhance the department’s process and procedures to support the organization’s growth. For full job description, click here.
Reporting to Fractyl’s President, the Clinical Project Manager provides leadership on the design, initiation and execution of clinical studies to support both product approvals and market adoption of company products. Responsibilities include the initiation and conduct of clinical studies globally with the Fractyl DMR system (Duodenal Mucosal Resurfacing) in the treatment of Type II Diabetes. As a key member of the team, this individual plays a crucial role to establish the Clinical team’s structure in support of Fractyl’s growth and expansion. With hands-on experience, the Clinical Project Manager collaborates with internal and external groups to support the Clinical team’s global initiatives. For full job description, click here.
For more information or to apply, please contact firstname.lastname@example.org. If you don’t see a position that fits your background, we are always happy to receive resumes from great candidates.
We value our agency partnerships, and from time to time solicit their assistance in identifying suitable candidates for our available opportunities. As such, unsolicited agency submissions will not be honored. We promote diversity and are proud to be an Equal Employment Opportunity employer. Fractyl participates in E-Verify.