Director, Regulatory Affairs
Quick Summary
The Director, Regulatory Affairs will lead global regulatory strategy for development-stage neuroscience programs.
Works with the Sr Director, Regulatory Affairs to develop and direct innovative and effective regulatory strategies in support of assigned MapLight portfolio projects.
Responsibilities
~1 min read- →Works with the Sr Director, Regulatory Affairs to develop and direct innovative and effective regulatory strategies in support of assigned MapLight portfolio projects.
- →Provides advice on regulatory issues and actively collaborates with cross-functional team members, e.g., Clinical Pharmacology, Toxicology, Research, Clinical Development, Biostats, Data Management, Quality, CMC, Pharmacovigilance, Medical Writing, Commercial, publishing vendor, consultants, etc.
- →May represent MapLight as point of contact with FDA and provides support for and coordination of regulatory meetings and briefing document development.
- →Provide regulatory guidance on clinical development plans, CMC strategies, and nonclinical programs to ensure regulatory alignment.
- →Lead or oversee the preparation and submission of regulatory documents, including INDs/CTAs, meeting packages, orphan drug applications, and other global regulatory filings.
- →Interpret and communicate regulatory requirements and risks to internal teams and senior leadership.
- →Monitor changes in the regulatory landscape relevant to neuroscience and provide strategic advice to adapt plans accordingly.
- →Collaborate with external partners, consultants, and regulatory agencies to advance development programs.
Requirements
~2 min read- Advanced degree (PhD, PharmD, MD, or MS) in life sciences or related field preferred.
- Minimum of 10 years of regulatory affairs experience in the biotechnology or pharmaceutical industry, with a focus on clinical-stage products.
- Experience in regulatory strategy for neuroscience or CNS therapeutics is highly preferred.
- Demonstrated success leading regulatory submissions and interactions with global health authorities.
- Strong understanding of global regulatory frameworks (e.g., FDA, EMA, ICH).
- Proven ability to influence cross-functional teams and drive strategic outcomes.
- Excellent written and verbal communication skills.
- Ability to work independently and thrive in a fast-paced, evolving environment.
Location: Remote US position. This is a hybrid in office position if you are located within 50 miles of either Redwood City, CA or Burlington, MA.
MapLight does not accept unsolicited resumes from recruiters, staffing agencies, or search firms.
Compensation for this role may vary within the above range based on many factors including geographic location, candidate experience, and skills. Additional compensation/benefits include annual bonus opportunity, medical, dental, vision, life and AD&D, short term and long term disability, 401(K) plan with match, stock options, flexible non-accrual paid time off, and parental leave.
EEOC Statement: MapLight Therapeutics is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability status, protected veteran status, or any other characteristic protected by law.
Listing Details
- Posted
- March 27, 2026
- First seen
- March 26, 2026
- Last seen
- April 17, 2026
Posting Health
- Days active
- 22
- Repost count
- 0
- Trust Level
- 43%
- Scored at
- April 17, 2026
Signal breakdown
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