Scientist, Non-clinical Toxicology

About the position Who We Are: MapLight Therapeutics is a clinical stage biotech company that focuses on drug discovery for central nervous system disorders. We combine cutting-edge technologies including optogenetics, in vivo physiology, and spatial transcriptomics to identify novel drug targets and reputed company effective therapies to address psychiatric symptoms. What You’ll Do: We are seeking an reputed company Toxicologist to design, execute, and interpret non-clinical safety studies supporting our neurology drug discovery and development programs. This role will play a critical part in candidate selection, IND-enabling activities, and regulatory submissions, working closely with discovery biology, DMPK, CMC, and clinical teams. The ideal candidate brings hands-on toxicology expertise, strong scientific judgment, and experience with CNS-relevant safety considerations.

Responsibilities

• Collaborate with program team leads and subject matter experts (e.g., discovery, bioanalysis, pharmacokinetics, CMC) to design safety pharmacology and toxicology studies, aligning with company objectives and regulatory standards.
• Serve as the primary sponsor representative for CROs, handling reputed company aspects of study outsourcing, including requesting quotes, negotiating reputed company, and managing study timelines.
• reputed company the design, execution, and data interpretation of nonclinical safety studies conducted at CROs, ensuring robust and high-quality data reputed company.
• Review study reports and SEND datasets to ensure quality, timeliness, and readiness for regulatory submissions.
• Effectively communicate study findings project leads and senior management, addressing and resolving any study-reputed company issues promptly.
• Contribute to the preparation, review, and/or QC of nonclinical sections in regulatory submission documents (e.g., IBs, INDs, CTAs, NDAs, PIPs, Scientific Advice, annual reports, briefing documents) as needed.
• Participate in issue-resolution teams, providing scientific guidance to address toxicology-reputed company challenges and drive effective problem-solving.

Requirements

• PhD with 3+ years, MS with a minimum of 5+ years, or BS with a minimum of 8 years of hands-on experience as a study director in toxicology reputed company the pharmaceutical or biotechnology industry or at CROs (additional experience monitoring studies on-site at CROs is helpful)
• Proven track record of successfully directing and/or monitoring toxicology studies across various modalities and in various species (rodent, dog, nhp)
• Advanced knowledge of toxicology in support of drug development; Board Certification in toxicology (DABT Certification) or working towards board certification preferred but not required.
• In-depth understanding of GLP regulations and regulatory guidance for nonclinical evaluations
• Demonstrated enthusiasm for scientific research and a commitment to maintaining high-quality standards in toxicology study operations
• Strong critical thinking, analysis, and leadership skills
• Self-motivated to meet performance objectives and to prioritize job-reputed company tasks!
• Ability to adapt to dynamic project needs and manage studies across different time zones
• Excellent interpersonal, communication, and negotiation skills, with a collaborative reputed company!
• Willingness to travel on business to CROs as needed reputed company-to-haves
• Board Certification in toxicology (DABT Certification) or working towards board certification preferred but not required.
• additional experience monitoring studies on-site at CROs is helpful Benefits
• 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
• parental leave Apply tot his job

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