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Senior Director, Clinical Development
Job in
San Francisco, San Francisco County, California, 94199, USA
Listed on 2026-08-02
Listing for:
Annexonbioscience
Full Time
position Listed on 2026-08-02
Job specializations:
-
Business
Regulatory Compliance Specialist
Job Description & How to Apply Below
About the Company
Annexon Biosciences is a biopharmaceutical company advancing a late-stage clinical platform of novel therapies to treat complement-mediated neuroinflammatory diseases.
PositionThe Sr. Director of Clinical Development will lead the clinical strategy and execution of one or more development programs, overseeing design and execution from Phase I through Phase III.
Responsibilities- Lead the strategic direction and execution of clinical development programs, from early-phase through late-stage trials, ensuring scientific robustness and regulatory compliance.
- Collaborate cross‑functionally with clinical operations, regulatory affairs, medical affairs, pharmacovigilance, and biostatistics to execute clinical plans.
- Drive regulatory filings, including trial applications, investigator brochures, and study protocols in accordance with FDA and EMA guidelines.
- Analyze, interpret, and communicate trial data to inform key decisions and provide recommendations.
- Establish and maintain strategic relationships with KOLs, investigators, and external stakeholders.
- Manage budgets, timelines, and resources to deliver high‑quality results aligned with corporate objectives.
- Present clinical progress, data outcomes, and strategic recommendations to executive leadership and stakeholders.
- Stay current on industry trends, scientific advances, and regulatory developments.
- Identify risks in timelines, budgets, or regulatory pathways and develop contingency plans.
- MD or PhD in Neurology, Neuroscience, or related field.
- Over 10 years of clinical development experience with CNS indications.
- Proven leadership in designing, managing, and executing trials from early to late stages.
- Experience leading clinical development teams at a senior/executive level, preferably in a high‑growth biotech or pharma.
- In‑depth knowledge of global regulatory requirements (FDA, EMA) and process, including experience with HA meetings, briefing books, and supporting meetings.
- Exceptional leadership, strategic thinking, and communication skills to influence across functions.
- Ability to work effectively in a fast‑paced, dynamic environment and manage multiple priorities.
- Strong analytical and problem‑solving skills with a data‑driven approach to decision making.
- Track record of building collaborations with cross‑functional teams and external partners.
- Experience with regulatory submissions and trial oversight in biotech or pharmaceutical settings.
- Familiarity with emerging neurology trends and novel therapeutic modalities.
$336,000 – $374,000.
LocationBrisbane, California (San Francisco Bay Area preferred).
Benefits- Flexible work schedules and remote opportunities for work‑life balance.
- Shuttle service from BART, Cal Train, and Ferry.
- Competitive base salary, equity participation, employee stock purchase plan, and comprehensive health benefits including medical, dental, vision, 401(k), flexible spending, and other benefits.
Annexon Biosciences is an Equal Opportunity Employer. We prohibit discrimination or harassment of any kind and foster an inclusive culture that respects individual strengths, views, and experiences.
#J-18808-LjbffrPosition Requirements
10+ Years
work experience
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