Effectively manage assigned Investigator sites and maintain positive relationships with site personnel.
Prepare for and conduct Pre-Study, Initiation, Interim and Closeout monitoring visits in accordance with MapLight SOPs, regulatory requirements, and ICH GCP.
Support the study team in meeting study milestones such as site activation, DSMB meetings, and database lock.
Perform centralized monitoring activities to ensure timely resolution of action items and oversight of study data quality.
Maintain quality and compliant documentation including monitoring visit reports, site contact reports, and TMF/ISF maintenance.
Serve as the main point of contact for Investigator sites to support protocol compliance and training needs.
Support the study team and Investigator sites during inspections or audits as needed.
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About MapLight Therapeutics
MapLight Therapeutics is pioneering new treatments for brain disorders. You will develop therapies that transform lives for conditions like schizophrenia, Alzheimer's, and Parkinson's. We combine single-cell transcriptomics, optogenetics, and spatial transcriptomics to discover novel drug targets. Our platform enables more effective and better-tolerated therapies. You will work on clinical-stage assets, including ML-007C-MA in Phase 2 for schizophrenia and Alzheimer's disease psychosis. Another promising compound, ML-004, is in Phase 2 trials for Autism Spectrum Disorder. We are also building a robust preclinical pipeline for other neurological conditions. MapLight has secured over $372.5 million in Series D funding from top investors, demonstrating strong confidence in our mission and approach.
How We Work
We foster a culture of rigorous science, transparency, and integrity. You will inspire, mentor, and support your colleagues in a collaborative environment. Our team members often work remotely, with some roles being fully remote across the US. For specific roles, a hybrid workspace might involve coming into our Redwood City, CA, or Burlington, MA offices three days a week. We empower you to make a significant impact on groundbreaking scientific discoveries. Teams operate with mutual respect, working together to evolve our organization. You will find a supportive atmosphere for professional growth and achievement.
Why Join Us
Contribute to treatments for severe brain disorders like schizophrenia and Alzheimer's.
Work with cutting-edge technologies including optogenetics and single-cell transcriptomics.
Join a well-funded company with over $372.5 million in Series D financing.
Experience a collaborative culture that values rigorous science and mutual support.
Benefit from comprehensive perks and flexible work options, including remote roles.
Benefits & Perks
Competitive salary ranges from $319,000 to $361,000 for a Senior Medical Director role.
Annual bonus opportunity and stock options.
Comprehensive medical, dental, and vision insurance.
Life and AD&D, short-term and long-term disability.
401(K) plan with company match.
Flexible non-accrual paid time off and parental leave.