Medical Director – FSP

This is a fully remote position, open to applicants in United States.

📋 Description

• Act as the Global Clinical Lead and medical monitor for one or more studies, including active participation in clinical subteams.

• Directly contribute as an author to protocols, clinical study reports, study documents, regulatory documents, and external publications.

• Conduct medical reviews of clinical trial data and provide medical monitoring for clinical trials.

• Engage with senior management regarding data presentations, trial updates, and strategic or executional development matters.

• Participate in strategic discussions concerning clinical development plans and prioritization of indications.

• Collaborate with clinical operations to manage and coordinate the operational aspects of ongoing projects, ensuring that time, cost, and quality objectives are achieved.

• Ensure that Clinical Development SOPs enable effective clinical research programs and comply with clinical/medical and industry standards.

• Critically assess and contribute to regulatory documents and interactions as necessary.

• Work cross-functionally to address trial issues and execution with partners across various departments.

⛳️ Requirements

• MD degree is required.

• Residency training in psychiatry is mandatory.

• Extensive experience in drug development within psychiatry, specifically in Phase 1–3 clinical development.

• Background in schizophrenia, bipolar disorder, ADHD, and major depressive disorder indications.

• A minimum of 5 years of experience in the pharmaceutical industry in a clinical development capacity as a Medical Director or Senior Medical Director.

• Exceptional written and verbal communication skills, including experience presenting to senior management and external stakeholders.

• Capability to navigate complexity and ambiguity in a highly matrixed work environment.

• Strong leadership and interpersonal skills for effective collaboration.

• Ability to work autonomously, efficiently prioritize tasks, and adhere to deadlines.

• Competence in conducting thorough and timely reviews of medical and trial-related documents.

🏝️ Benefits

• Competitive salary and performance-based bonuses.

• Comprehensive health, dental, and vision insurance.

• Generous paid time off and holiday policies.

• Opportunities for professional development and continuing education.

• Flexible work arrangements to support work-life balance.