Part-Time Study Coordinator

Position Details

Job Title RESEARCH COORDINATOR Position Number 8350277 Work Modality Fully Remote Work Is this request for the creation of a new Position (or the modification of an existing Position) to temporarily support the Work Day ERP? No Job Category University Staff Job Type Part-Time FLSA Status Non-Exempt Campus Maywood-Health Sciences Campus Department Name SCHOOL OF NURSING Location Code SCHOOL OF NURSING (02400A) Is this split and/or fully grant funded?

Yes Duties and Responsibilities

Position Summary

The Study Coordinator provides leadership for the operational, administrative, and regulatory management of federally funded behavioral and clinical research studies. Working closely with the Principal Investigator and Co-Investigators, the Study Coordinator oversees study implementation, supervises research personnel, ensures regulatory compliance, manages project timelines and budgets, and supports dissemination of research findings.

Duties and Responsibilities

Study Leadership & Participant Engagement

* Coordinate the daily operations of the research study.

* Develop and implement participant recruitment, enrollment, and retention strategies.

* Oversee participant recruitment, scheduling, retention, and completion of study activities.

* Oversee participant compensation activities and ensure compliance with institutional and sponsor requirements.

* Support community engagement and incorporate feedback from consultants including parent advisory council to inform research procedures.

Study Implementation & Data Collection

* Direct implementation of study protocols, including surveys, interviews, EMA, and family interaction procedures.

* Oversee development and management of electronic surveys, EMA programming, study databases, and participant tracking systems.

* Supervise preparation and distribution of study materials.

* Conduct virtual study visits and ensure protocol fidelity.

Personnel Management

* Train, supervise, mentor, and evaluate research staff and student personnel.

* Conduct regular research team meetings and provide ongoing training.

Data Management & Quality Assurance

* Oversee study data collection, coding, quality assurance, storage, security, reproducibility, and documentation.

* Monitor study operations and implement quality control procedures.

Regulatory & Administrative Oversight

* Oversee informed consent and assent procedures.

* Prepare and submit IRB applications, amendments, continuing reviews, adverse event reports, and other regulatory documents.

* Develop and maintain study documentation, SOPs, and regulatory files.

* Manage project timelines, monitor deliverables, and communicate study progress with investigators.

Research Dissemination & Communication

* Coordinate preparation of abstracts, manuscripts, grant reports, and presentations.

* Support dissemination of research findings through conferences, publications, and community engagement.

* Oversee development and maintenance of the study website to ensure timely, accurate, and accessible study information.

Other Responsibilities

* Perform other duties as assigned.

Minimum Education and/or Work Experience

* Minimum of Bachelor's degree in nursing, public health, psychology, health sciences, social work, or another health-related field; or an equivalent combination of education and relevant experience.

* Minimum of three to five years of progressively responsible experience coordinating clinical, behavioral, community-based, or federally funded research studies.

Qualifications

Required Qualifications

* Bachelor's degree in nursing, public health, psychology, health sciences, social work, or another health-related field; or an equivalent combination of education and relevant experience.

* Minimum of three to five years of progressively responsible experience coordinating clinical, behavioral, community-based, or federally funded research studies.

* Demonstrated experience coordinating multiple research activities, including participant recruitment, enrollment, retention, data collection, and study implementation.

* Experience supervising, training, mentoring, or providing day-to-day direction to research staff, students, or project personnel.

* Demonstrated knowledge of human subjects research regulations, Institutional Review Board (IRB) requirements, informed consent procedures, and research ethics.

* Availability to work a flexible schedule, including occasional evenings and weekends, to support participant activities and community engagement events as needed.

Preferred Qualifications

* Bachelor's or graduate degree in nursing (BSN, MSN, DNP, PhD or equivalent) preferred.

* Experience working with individuals and families living with spina bifida or other chronic health or complex care condition.

* Bilingual proficiency in English and Spanish is preferred.

Certificates/Credentials/Licenses

Bachelor's degree in nursing, public health, psychology, health sciences, social work, or another health-related field; or an equivalent combination of education and relevant…