About this opportunity
Villanova University lists this Project Director opportunity in rosemont, Pennsylvania. Review the employer’s description below for duties, qualifications and application requirements.
Job description
Villanova University
Project Director
Posting Details
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Job Information
Posting Number: S
Position Title: Project Director
Position Type: Staff
Location: Villanova, PA
Recruitment Type: Internal/External Applicants
Work Schedule: full-time/12-months
Avg Hours Week:
Department: 948-Nursing-Research & Innovation
Position Summary
Villanova's Fitzpatrick College of Nursing seeks an experienced and organized full-time Project Director to lead operations for an NIH-funded, multi-site mixed methods study focused on improving outcomes for lung transplant patients and caregivers (R01HL , Principal Investigator Brittany Koons). The Project Director will serve as the operational lead across collaborating institutions and will work closely with the Principal Investigator to drive study execution, regulatory compliance, participant engagement, and cross-site coordination.
The Project Director will be responsible for administrative aspects and day-to-day operations of the study, as well as other duties assigned which support the launch and maintenance of the study. This position is a hybrid position with most work time being remote with periodic on-site time required for staff trainings.
Villanova is a Catholic university sponsored by the Augustinian Order. The University is an equal opportunity employer and seeks candidates who understand, respect and can contribute to the University's mission and values.
Duties and Responsibilities
Regulatory and Compliance
Lead IRB submissions/modifications across participating sites
Manage data use agreements between Villanova and all study sites
Serve as the primary liaison for Villanova's research administration for all grant-related administration needs.
Oversee grant budget management, resource allocation, project tracking, and preparation of progress reports.
Study Operations
Monitor recruitment, enrollment, and longitudinal follow-up (e.g., schedule study visits)
Conduct virtual study visits as needed
Coordinate multi-site research activities and timelines and ensure protocol compliance
Set up and manage project in REDCap
Prepare qualitative recordings for analysis in NVivo
Implement protocols to capture missing survey data
Manage incoming data transfers
Manage participant compensation
Team Leadership
Train and supervise research assistants and site coordinators
Facilitate investigative meetings and cross-site communication
Assist PI with reporting, manuscript preparation, and dissemination activities
Minimum Qualifications
Formal Education
Bachelor's degree in nursing, social work, psychology, public health or related field
Work Experience
At least 5 years of experience in research and academic environments as a project/program manager or an equivalent combination of education and experience required.
Experience managing federally funded, patient-oriented clinical research studies, preferably longitudinal and multi‑site studies
Demonstrated success supervising and coordinating research staff, including research assistants and study coordinators.
Experience overseeing IRB submissions, regulatory compliance activities, and research documentation across study sites.
Experience monitoring grant budgets, resource allocation, and study timelines to support successful project execution.
Work Skills (e.g., written and verbal communication skills)
Ability to manage high‑priority situations with professionalism, sound judgment, and composure
Outstanding written and verbal communication skills, including the ability to effectively coordinate across multidisciplinary research teams and collaborating institutions.
Strong organizational, critical thinking, and project management skills with exceptional attention to detail
Demonstrated ability to independently manage complex research operations while balancing multiple projects and deadlines
Excellent interpersonal skills with the ability to build collaborative working relationships with investigators, research staff, participants, and external partners
Demonstrated professionalism, discretion, and commitment to maintaining confidentiality and regulatory compliance related to patient and research data
Ability to adapt to evolving study needs and efficiently learn new technologies, systems, and research procedures
Ability to analyze problems, develop solutions, and proactively address operational challenges in a dynamic research environment
Specific Job Knowledge (e.g., knowledge of principles and procedures related to field and area)
Knowledge of principles and compliance requirements of the Health Information Privacy and Portability Act (HIPPA) and its relevance in healthcare-related research
Knowledge of procedures for participant screening and consent
Knowledge of processes related to study and grant management
Equipment Knowledge
Microsoft Office Suite
Design Software (e.g., Canva, Adobe Creative Suite)
Remote meeting software (e.g., Zoom, Microsoft Teams)
Data management software (e.g. LabArchives, DropBox, OneDrive, SharePoint, REDCap, NVivo)
Reference management tools (e.g. Covidence, EndNote)
Task Management and project tracking software (e.g., Norton, Asana)
Preferred Qualifications
Formal Education
Master's degree in nursing, social work, psychology, public health or related field
Work Experience
More than 5 years of experience managing complex clinical research projects within academic medical centers, healthcare systems, or research‑intensive environments
Experience supporting NIH-funded or other federally funded research programs, including familiarity with NIH reporting requirements and sponsor compliance expectations
Experience coordinating longitudinal, multi‑site, and/or mixed methods research studies
Experience managing patient-caregiver dyadic or other family‑centered research studies
Experience supporting qualitative and survey‑based data collection, management, and analysis
Experience contributing to scientific dissemination activities, including manuscripts, conference abstracts, presentations, and research reports
Experience overseeing clinical research data management activities, including data quality monitoring, data cleaning, cross‑site query resolution, preparation of study reports, and collaboration with statistical teams to support data analysis
Specific Job Knowledge (e.g., knowledge of principles and procedures related to field and area)
The Collaborative Institutional Training Initiative (CITI) Program certification preferred
Physical Requirements and/or Unusual Work Hours
May require some evenings and/or weekends, scheduled ahead of time
Job could involve sitting for one or more hours on the computer; however, the Project Director can schedule breaks and/or move as needed
Posting Date
09/10/2026
Closing Date (11:59pm ET)
Salary Posting Information
This position falls within salaried grade 16 and the range is $73,100-91,400. The final salary will be determined with consideration of several factors including the selected candidate's qualifications, department budget availability, market data, and internal equity.
Salary Grade
16
Job Classification
exempt
References Needed
Minimum Number of References Needed 3
Maximum Number of References Needed 3
Supplemental Questions
Required fields are indicated with an asterisk (*)
Documents needed to complete your application:
Required Documents Cover Letter / Letter of Interest
Resume / Curriculum Vitae
Optional Documents Letters of Reference (uploaded by applicant)
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Who can apply
Review the original listing for work authorization, qualifications and employer requirements.