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Research Director – National Women’s Health Platform

12/10/2025

The Research Director will support and coordinate clinical research activities across multi-site studies and prepare and maintain IRB protocols. They will also analyze clinical data and contribute to research manuscripts and presentations.

Working Hours

40 hours/week

Company Size

51-200 employees

Language

English

Visa Sponsorship

About The Company

Persistent pelvic pain impacts 15% of women and 10% of men throughout their lifetime. This disease process has been misdiagnosed, undertreated, ignored, and silenced. There is a better way to provide the quality of life that our patients deserve. The better way is here. We believe that the millions of women and men who suffer from pelvic pain should have access to care that provides relief. We don’t believe “a glass of wine will fix it” or that “it’s all in your head”. We will never abandon you – and from leadership to the front office to every pelvic pain specialist you meet, so much of our team has been in your shoes and believes the pelvic pain patient deserves better. This belief is what unifies us all at Pelvic Rehabilitation Medicine. Since 2017, PRM has provided an innovative solution to a health crisis that affects 15% of women and 10% of men. Persistent pelvic pain is often overlooked, untreated, and misguided. At PRM, our mission is to decrease the time patients are suffering from pelvic pain symptoms. We offer a proprietary, simple, office-based procedure to treat the symptoms of chronic pelvic pain. The PRM Protocol™ consists of a series of pelvic nerve and muscle treatments to directly target inflammation in the pelvis and nerve pain. Depending on the condition causing your pelvic pain, other modalities may be needed in addition to our treatment.

About the Role

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

Key Skills

Clinical ResearchIRB ComplianceData AnalysisStatistical AnalysisResearch ManuscriptsCollaborationData GovernanceHIPAA ComplianceOrganizational SkillsCommunication SkillsTime ManagementAttention to DetailElectronic Data CaptureClinical Outcome MeasuresPatient-Reported Data Analysis