Lead and manage a team of Clinical Research Associates, providing line management, performance management, and career development.
Maintain site management and monitoring responsibility for at least one site, including conducting pre-study, initiation, interim, and closeout visits.
Ensure study team compliance with internal procedures and regulatory requirements (GCP).
Develop and maintain the study monitoring plan, templates, and tools, implementing strategies based on study design and recruitment goals.
Act as a core member of the cross-functional study team, providing expertise on monitoring processes and participating in risk management.
Review monitoring visit reports and Key Performance Indicators to ensure quality standards and performance compliance.
Support site management documentation, including Trial Master File (TMF) and Investigator Site File (ISF) maintenance.
Support internal and external stakeholders during inspections or audits.
GCP
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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.