Medical Director / Senior Medical Director at Neumora

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Full Time

Start Date

Immediate

Expiry Date

14 Oct, 26

Salary

367934.0

Posted On

16 Jul, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical Development, Medical Oversight, Patient Safety, Protocol Adherence, Data Analysis, Regulatory Documentation, Clinical Development Plans, Precision Phenotyping, KOL Engagement, Study Site Identification, Risk-based Decision Making, Cross-functional Leadership

Industry

Biotechnology Research

Description

At Neumora, we are pushing the boundaries of science and technology to revolutionize the way patients with brain disease are treated. We are seeking extraordinary individuals to join our team as we grow and advance our pipeline. The Medical Director/Senior Medical Director provides oversight of the medical and scientific aspects of Neumora clinical studies and works closely with counterparts in clinical operations and statistics in ensuring high quality study conduct. In addition, they interact cross-functionally with discovery, biology, toxicology, translational and data science groups to provide medical insights and promote integration of precision medicine strategies in Neumora’s development programs. Responsibilities: Provides clinical development and medical leadership/oversight of clinical programs to ensure timely delivery of clinical deliverables. Ensures clinical programs support patient safety and provides oversight of patient safety in clinical studies. As the primary medical expert for assigned study(ies), they are the first point of contact internally and externally for questions regarding the study (e.g. eligibility, enrollment; safety and patient management). Monitors study progress to ensure proper study conduct and adherence to the protocol, leads data review, evaluation, and analyses with support from the cross functional team. Takes a key role in the authoring of critical study documents (e.g., CSR, IB, protocol synopsis). Contributes to the analysis and interpretation of data generated internally or externally and present study updates, interim results, and final headline data to senior management as required. Provides medical input and contributes to the clinical development sections of regulatory documents such as IND, CIOMS, DSUR, Dossiers, and contributing to responses to regulatory agencies regarding questions about complex clinical development issues (e.g., safety or efficacy). Contributes to the cross functional development of clinical development plans (CDPs) that integrate pre-clinical, early clinical findings and data sciences approaches - working to ensure cross-functional alignment on an ongoing basis throughout the phases of clinical development. Collaborates with teams on the development of translational and precision phenotyping strategies and contributes to the design of scientifically rigorous clinical development studies and programs utilizing a data biopsy signature/precision phenotype approach. Ensures that teams appreciate the clinical relevance and applicability of the approaches considered. Identifies and engages with external Key Opinion Leaders to address scientific and medical questions relevant to the program. Helps identify global study sites and foster relationships with study investigators. Ensures that Serious Adverse Events are properly reported. Implements clinical R&D policies, SOPs, and related directives. As required, supports any needed due diligence of potential in-licensing drug candidates and/or technologies and present recommendations to leadership. Qualifications: MD required; Ph.D. and/or board certification in psychiatry preferred Active medical license desirable 3+ years of relevant experience as a Medical Director in the biotech or pharmaceutical industry or equivalent Psychiatry drug development experience required, Psychogeriatric or Neurodegeneration development experience a plus. Experience in leading medical and scientific aspects of clinical studies on cross functions teams Ability to critically review, analyze and interpret key aspects of clinical study conduct, including research design, methods, and outcome measures, is required. Ability to work in a remote environment and with distributed teams; startup experience preferred Effective communication skills to enable engaging and influencing diverse stake holders from a variety of professional backgrounds Ability to navigate complexity and make risk-based decisions Self-starter who can independently lead assigned projects Demonstrated ability to engage and influence diverse stakeholders from a variety of professional backgrounds 2026 Company benefits include: Medical, dental, vision, and life insurance 401(k) plan: Neumora matches 50% of an employee’s eligible contribution, up to the first 6% of salary (up to 3% employer contribution) Company Equity (New Hire Awards, Annual Awards, ESPP) Annual paid time off: Accrued Vacation Days: 15 days per year Sick Days: 10 days per year Company Holidays: 13 days plus summer recharge week in July and winter shutdown in December Leave of Absence: Paid Medical Leave, Paid New Parent Bonding Leave, Paid Family Leave, paid short-term and long-term disability Discretionary year-end bonus The salary range posted describes the minimum to maximum base salary range for this position in the location listed. Actual salary may vary based upon geographic location, work experience, education, licensure requirements and/or skill level and will be finalized at the time of offer. Base Salary Range:$289,800-$367,934 Neumora Therapeutics, Inc. is a clinical-stage biopharmaceutical company founded to confront the greatest medical challenges of our generation by taking a fundamentally different approach to the way treatments for brain diseases are developed. Our therapeutic pipeline currently consists of seven programs that target novel mechanisms of action for a broad range of underserved, prevalent diseases. Neumora’s mission is to redefine neuroscience drug development by bringing forward the next generation of novel therapies that offer improved treatment outcomes and quality of life for patients. Neumora is an equal opportunity employer and will not discriminate against any employee or applicant on the basis of age, color, disability, gender, national origin, race, religion, sexual orientation, veteran status, or any classification protected by federal, state, or local law.

Responsibilities

Provides medical and scientific oversight for clinical studies to ensure high-quality conduct and patient safety. Collaborates cross-functionally to integrate precision medicine strategies and author critical regulatory and study documents.