Senior Associate, Regulatory Affairs

MapLight Therapeutics is seeking a Senior Associate in Regulatory Affairs to join our team dedicated to developing therapies for central nervous system disorders. This role involves supporting regulatory activities to advance our clinical-stage programs.

The Senior Associate will assist the Regulatory Lead with IND/CTA submissions and agency meetings, maintain regulatory documentation, and collaborate with CROs and partners to support clinical study activities. Responsibilities include drafting forms and cover letters, archiving regulatory documents, and monitoring new regulatory requirements.

Candidates should have a Bachelor's degree in a scientific discipline, with a minimum of 2 years in the pharmaceutical industry. Strong interpersonal, written, and verbal skills are essential, along with the ability to understand and communicate scientific information. Experience in planning, organizing, and prioritizing multiple activities is also required.

This hybrid position requires three days per week onsite at our offices in Burlington, MA, or Redwood City, CA. Compensation includes an annual salary ranging from $87,000 to $114,000, along with benefits such as annual bonus opportunities, medical, dental, vision, life and AD&D insurance, short-term and long-term disability, 401(K) plan with match, stock options, flexible non-accrual paid time off, and parental leave.

Joining MapLight Therapeutics offers the opportunity to be part of a collaborative team focused on innovative drug discovery for psychiatric symptoms. We value integrity, collaboration, bravery, and dedication, providing a dynamic environment for professional growth.