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.

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