Medical Director, Medical Affairs – Psychiatry (U.S., Remote)
Company: Worldwide Clinical Trials – USA
Location: United States (Remote, Home-Based)
Salary: Competitive
Start Date: December 9, 2025
Closing Date: January 8, 2026
Experience Required: Minimum 2+ years in CRO Medical Monitoring
About Worldwide Clinical Trials
Worldwide Clinical Trials is a global mid-sized CRO committed to pioneering clinical research for some of the world’s most challenging diseases. With a team of 3,500+ professionals, we combine scientific excellence with creativity to deliver innovative solutions that improve patient outcomes globally.
Our mission is to advance patient care and research while fostering a collaborative, inclusive, and diverse workplace. At Worldwide, every professional has the opportunity to make a meaningful impact on the lives of patients and caregivers worldwide.
Role Overview
As a Medical Director – Psychiatry, you will play a critical role in Medical Affairs, contributing across the full lifecycle of clinical investigations. From protocol development and feasibility assessments to medical monitoring, pharmacovigilance, and study report preparation, you will ensure scientific integrity, patient safety, and regulatory compliance.
This remote position provides an opportunity to lead, mentor, and collaborate with cross-functional teams while shaping the medical strategy for psychiatry-focused clinical trials.
Key Responsibilities
Provide medical oversight and input for clinical trial protocols, design, and execution.
Collaborate with Medical & Safety teams to process Serious Adverse Events (SAEs).
Contribute to business development activities, including proposal generation, feasibility assessments, and sponsor meetings.
Review and assist in the preparation of Clinical Study Reports (CSRs), protocols, ISS/ISEs, and other regulatory documentation.
Maintain up-to-date knowledge of therapeutic advancements, clinical research literature, and market developments.
Mentor and support junior medical staff, promoting best practices, integrity, and scientific excellence.
Support internal and external collaborations with sponsors, investigators, and cross-functional project teams.
Qualifications & Skills
Medical Degree (MD/DO) with a specialization in Psychiatry from an accredited institution.
Minimum 2 years of medical monitoring experience in a CRO environment.
Strong understanding of clinical research, regulatory guidelines, and patient safety principles.
Excellent written and verbal English communication skills.
Proficiency in Microsoft Office Suite (Word, Excel, Access).
Outstanding organizational, presentation, and time management skills.
Valid passport and willingness to travel as required.
Why Join Worldwide Clinical Trials?
Work remotely while impacting psychiatric patient outcomes globally.
Collaborate with experienced, cross-functional teams in innovative clinical trials.
Thrive in a diverse and inclusive environment that encourages creativity, professional growth, and collaboration.
Be part of a mission-driven organization committed to scientific excellence and improving patient lives.
Equal Opportunity Employer
Worldwide Clinical Trials is an equal opportunity employer, committed to fostering a workplace that is inclusive, diverse, and supportive. All qualified applicants will receive consideration regardless of race, color, ethnicity, gender, religion, age, disability, military status, or other legally protected characteristics.
Apply Now
Contribute to transforming patient lives in psychiatry by joining Worldwide Clinical Trials. Explore more career opportunities at Worldwide Clinical Trials Careers and connect with us on LinkedIn.
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