Research Director – National Women’s Health Platform

Description Organization: Pelvic Rehabilitation Medicine (PRM) Position Type: Full-Time Location: Remote (Must reside in one of the following states: California, Florida, Georgia, Illinois, Maryland, Michigan, New Jersey, New York, Ohio, Tennessee, Texas, Virginia) About Pelvic Rehabilitation Medicine Pelvic Rehabilitation Medicine (PRM) is a national leader in women’s health dedicated to advancing pelvic health through compassionate clinical care, data-driven research, and education. Our mission is to improve the quality of life for patients with chronic pelvic pain and pelvic floor dysfunction through evidence-based treatment and ongoing clinical research. Position Overview We are seeking a motivated and detail-oriented Research Director to support our expanding national women’s health research initiatives. The ideal candidate will have a strong background in clinical research, IRB compliance, and data analysis, and will contribute to advancing evidence-based practices through high-quality research and peer-reviewed publications. Key Responsibilities • Support and coordinate clinical research activities across multi-site studies within the PRM network. • Prepare, submit, and maintain Institutional Review Board (IRB) protocols and related documentation. • Collect, clean, manage, and analyze clinical data, ensuring data integrity and regulatory compliance. • Perform descriptive and inferential statistical analyses using Excel, Python, R, or SPSS as appropriate. • Contribute to research manuscripts, abstracts, and presentations for submission to peer-reviewed journals and conferences. • Collaborate with physicians, data scientists, and research leadership on study design, data governance, and quality control. • Develop reports and visualizations to present data outcomes and insights to internal stakeholders. • Support data governance initiatives to maintain compliance with HIPAA, IRB, and institutional data standards. Requirements Required: • Bachelor’s degree in a health sciences, biology, psychology, public health, or related field (Master’s preferred). • 1–3 years of experience in clinical research, including IRB submissions and regulatory documentation. • Proven experience contributing to peer-reviewed research publications. • Proficiency in data analysis and statistics using Excel and at least one programming language (Python or R). • Comfort working in SPSS for additional statistical analyses as needed. • Demonstrated experience cleaning, analyzing, and presenting clinical data. • Understanding of data governance and compliance principles (HIPAA, IRB, and ethical research conduct). • Strong organizational, communication, and time management skills with attention to detail. Preferred: • Familiarity with electronic data capture systems (e.g., REDCap, Qualtrics, or similar). • Knowledge of clinical outcome measures and patient-reported data analysis. Compensation & Benefits • Competitive salary commensurate with experience. • Comprehensive health, dental, and vision benefits. • Paid time off, holidays, and professional development opportunities. • Opportunity to contribute to impactful national women’s health research. How to Apply Interested candidates should submit a resume, cover letter, and sample of research work or publication Apply tot his job