Medical Director, Medical Affairs – Psychiatry (Remote, United States)
Employer: Worldwide Clinical Trials – USA
Location: United States (Remote)
Job Type: Full-Time
Category: Medical Affairs / Clinical Research / Psychiatry
Salary: Competitive
Application Deadline: 10 December 2025
Overview
Worldwide Clinical Trials, a leading global midsize CRO, is seeking an experienced Medical Director, Medical Affairs – Psychiatry to support clinical programs across the full lifecycle of clinical research. This fully remote role offers the opportunity to work within a highly collaborative, innovative environment focused on advancing psychiatric drug development.
With a global team of more than 3,500 professionals, Worldwide Clinical Trials is known for scientific excellence, operational quality, and transformative clinical solutions. This position plays a central role in shaping medical strategy, supporting clinical operations, and ensuring high-level scientific oversight.
Key Responsibilities
Medical and Scientific Leadership
Provide medical guidance across assigned clinical projects, ensuring scientific integrity and regulatory alignment.
Collaborate with Medical and Safety teams to process Serious Adverse Events (SAEs).
Deliver medical input for study protocols, development plans, research manuscripts, and white papers.
Strategic and Operational Support
Support Business Development through proposal contributions, feasibility assessments, and participation in sponsor meetings.
Assist in preparing and reviewing study documentation, including Clinical Study Reports (CSRs) and protocol-related materials.
Maintain strong knowledge of therapeutic advancements and project requirements through literature review and attendance at relevant conferences.
Cross-Functional Collaboration
Partner with internal departments to ensure alignment on project strategies and study execution.
Mentor junior medical staff and contribute to a culture of excellence, integrity, and scientific rigor.
Required Experience and Qualifications
Education
Medical Degree (MD or equivalent) from an accredited institution.
Specialization in Psychiatry is required.
Professional Experience
Minimum 2 years of medical monitoring experience within a CRO environment.
Strong understanding of clinical trial processes, safety reporting, and regulatory frameworks.
Experience contributing to protocol development, feasibility assessments, and scientific documentation.
Skills
Strong written and verbal communication skills in English.
Excellent organizational, analytical, and presentation abilities.
Proficiency in MS Office applications (Word, Excel, Access).
Ability to travel as needed; valid passport required.
Why Join Worldwide Clinical Trials
Worldwide Clinical Trials offers:
A diverse and inclusive work environment supporting career growth.
Opportunity to directly influence global psychiatric research and patient outcomes.
Engagement with innovative clinical programs and cross-functional scientific teams.
The organization is committed to equal employment opportunities and creating an inclusive workplace that promotes collaboration, creativity, and professional excellence.
How to Apply
Interested candidates may submit their application through the Worldwide Clinical Trials careers portal. Additional information about the organization and similar roles can be found at www.worldwide.com or via the company’s official LinkedIn page.
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