Principal Investigator – Women’S Health

Overview

• Lead clinical research studies in Women’s Health, focusing on reproductive, hormonal, and general health conditions.
• Provide medical direction and oversight for clinical trials, ensuring scientific integrity and regulatory compliance.
• Act as the site’s lead medical authority, overseeing participant safety and coordinating with sponsors.
• Collaborate with study monitors and sponsors to ensure successful execution of research protocols.
• Offer flexibility for full-time or part-time scheduling, supporting work-life balance.
• Contribute to advancing care and treatment for women in key therapeutic areas.
• Work in a dynamic environment with opportunities for professional growth and development.
• Engage in meaningful work that impacts patient care and clinical research advancements.

Key Responsibilities & Duties

• Provide medical leadership for Women’s Health research studies, ensuring adherence to study protocols and ethical standards.
• Conduct or supervise clinical trial procedures performed by research staff.
• Verify training, competency, and qualifications of research personnel.
• Ensure compliance with FDA, GCP, IRB regulations, and company policies.
• Review and interpret study data, including lab and imaging results.
• Oversee subject recruitment and retention efforts in collaboration with site coordinators.
• Mentor Sub-Investigators and clinical team members to foster professional growth.
• Provide weekend or after-hours oversight as required by study protocols.

Job Requirements

• Doctor of Medicine (MD) degree with specialization in Women’s Health, OB/GYN, Family Medicine, or Internal Medicine.
• Board-certified or board-eligible in Women’s Health or OB/GYN preferred.
• Minimum 2 years of clinical practice experience; research experience preferred but not required.
• Active physician license in Ohio, ensuring eligibility to practice.
• Strong clinical judgment and expertise in women’s health and reproductive care.
• Excellent organizational, leadership, and communication skills.
• Proficiency in Microsoft Office and clinical trial management systems.
• Compassionate approach to patient interaction and care.