Director, Regulatory Affairs at Septerna

South San Francisco, California, United States -

Full Time

Start Date

Immediate

Expiry Date

09 Feb, 26

Salary

260000.0

Posted On

11 Nov, 25

Experience

10 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Regulatory Affairs, Project Management, Communication Skills, Drug Development, Cross-Functional Leadership, Regulatory Strategy, IND Submissions, CTA Submissions, FDA Interactions, Risk Management, Collaboration, Attention to Detail, Mentoring, Strategic Thinking, Problem Solving

Industry

Biotechnology

Description

Septerna is a biotechnology company based in South San Francisco, CA on a mission to develop life-changing medicines for patients with the vision to become the industry-leading G protein-coupled receptor (GPCR)-focused drug discovery company. The company’s Native Complex Platform™ recapitulates GPCRs with their native structure, function, and dynamics outside of the cellular context. This approach enables novel access to modern structural and screening technologies used in industrial-scale drug discovery for the entire class of GPCRs. Septerna has an emerging pipeline of GPCR-targeted small molecule programs with potential for growth to target many GPCRs that have been undruggable and unexploited to date. We are excited to expand our multidisciplinary team of individuals focused on creating revolutionary medicines to address the unmet needs of patients. At Septerna we strive to embrace diversity of thought, expertise, and background through collaboration. To join our ambitious team, be prepared to bring your real self to work every day; grow and learn from a talented team of drug hunters, scientists, and business professionals; and contribute your passion, creativity, and energy to accomplish our mission. We share a fearless pursuit of ground-breaking innovations and cultivate an environment where our employees succeed by learning from each other and working as a team. We are committed to the development of meaningful therapeutics for patients with indications of high unmet need. This is a tremendous opportunity to work with talented individuals on the frontlines of therapeutic discovery and development. You will directly help move therapies through preclinical research, positioning them for success in the clinic. The successful candidate will add their passion, unique talents, and expertise to a dynamic team motivated to discover new disease-modifying therapeutics for patients in a fast-paced environment. For more information see: www.septerna.com. About the Role Septerna is seeking an experienced and highly motivated Director of Regulatory Affairs to lead regulatory strategy and execution across our discovery and development programs. This individual will be responsible for developing and implementing regulatory plans and submissions to support preclinical and clinical development, IND/CTA submissions, and interactions with global health authorities. The ideal candidate will bring deep regulatory expertise, strong cross-functional leadership, and a proactive, strategic mindset suited to a fast-paced biotech environment. This position reports into the VP, Regulatory Affairs. Responsibilities Develop and implement regulatory strategies for clinical stage programs, ensuring alignment with business and development objectives. Serve as the primary Regulatory Affairs representative on project teams, providing guidance on regulatory requirements and pathways. Lead the preparation, review, and submission of high-quality regulatory documents, including INDs, CTAs, amendments, briefing packages, and responses to health authority inquiries. Manage interactions with FDA and other global regulatory agencies; coordinate and prepare for regulatory meetings. Partner with CMC, Nonclinical, and Clinical teams to ensure compliance with applicable regulations and consistent messaging across submissions. Identify regulatory risks and proactively work with cross-functional teams to develop mitigation strategies. Monitor the evolving regulatory landscape and communicate implications for Septerna’s programs. Support the development of internal regulatory processes, systems, and documentation to enable scalability as the organization grows. Mentor and develop junior regulatory staff and contribute to a culture of collaboration and excellence. Qualifications Bachelor’s degree in life sciences or a related field; advanced degree (PhD, PharmD, or MS) preferred. Prior experience as a Global Regulatory Lead (GRL) preferred. 10+ years of experience in Regulatory Affairs within the biopharmaceutical industry, including direct experience leading IND and/or CTA submissions. Proven track record of successful interactions with the FDA and other global regulatory agencies. Strong understanding of drug development processes, from discovery through clinical stages. Excellent project management, organizational, and verbal and written communication skills. High attention to detail and accuracy. Ability to thrive in a dynamic, fast-paced environment and work effectively across functions. Hands-on, strategic thinker with a collaborative and solution-oriented mindset. The anticipated salary range for candidates who will work in South San Francisco, CA is $235,000 - $260,000. Individual pay may vary based on additional factors, including, and without limitation, job-related skills, experience, work location and relevant education or training. Septerna's compensation package also includes benefits, stock options, and annual target bonus for full-time positions. Note to Employment Agencies: Please do not forward any agency resumes. The company will not be responsible for any fees related to resumes that are unsolicited. We are an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status. Septerna participates in the E-Verify program. California Consumer Privacy Act Privacy Notice For Job Applicants. If you are a California resident, click here for our CCPA Notice.

Responsibilities

Lead regulatory strategy and execution across discovery and development programs. Develop and implement regulatory plans and submissions to support preclinical and clinical development.