FREE ACCESS
5,000–10,000 jobs/day
See all jobs on Scoutfield
Search thousands of fresh jobs every day.
Discover
- Fresh listings
- Fast filters
- No subscription required
Create a free account and start exploring right away.

Research Project Manager
Penn Information Systems & Computing. Provide day-to-day operational leadership and oversight for all aspects of the study .
Posted 11/3/2026full-timePhiladelphia • Pennsylvania • United StatesJuniorMid-Level💰 $67,155 - $74,327 per yearWebsite
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in managing clinical research operations, including regulatory compliance, participant recruitment, and qualitative research methodologies. Proficient in preparing reports and coordinating communication among stakeholders to ensure study success.
Highest-signal resume keywords
Regulatory And IRB SubmissionsParticipant Recruitment And RetentionQualitative Research And CodingHuman-Centered Design ActivitiesDescriptive Report Preparation
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Project Timeline DevelopmentStandard Operating ProceduresData Quality StandardsProtocol Deviations ManagementAdverse-Event DocumentationInformed Consent ProcessesQualitative Interview SupportTranscription ReviewIntervention Fidelity MonitoringDescriptive Report Preparation
Soft Skills
Operational LeadershipCommunication CoordinationTeam CollaborationProblem-SolvingLogistics Management
Industry Keywords
Mental Health ResearchClinical ResearchPsychologyNursingSocial WorkRCT ProceduresParticipant SchedulingFeedback SynthesisStudy ProtocolsData-Security Procedures
About the role
Key responsibilities & impact- Provide day-to-day operational leadership and oversight for all aspects of the study
- Develop and maintain project timelines, work plans, standard operating procedures, and tracking systems
- Coordinate staff workflows and monitor progress toward study milestones and deliverables
- Prepare and coordinate IRB submissions, amendments, continuing reviews, protocol deviations, adverse-event documentation, and progress reports
- Ensure study activities comply with approved protocols, institutional policies, and data-security procedures
- Coordinate participant recruitment, screening, informed consent, enrollment, scheduling, retention, and incentive tracking
- Maintain recruitment and retention logs and descriptive participant summaries
- Coordinate and support qualitative interviews, guided SVR walkthroughs, and follow-up interviews
- Review interview transcriptions, de-identify documentation, and conduct qualitative coding
- Support human-centered design and co-design mini-workshops, including materials, logistics, documentation, and feedback synthesis
- Support pilot RCT implementation, including participant orientation, VR-headset logistics, intervention scheduling, fidelity monitoring, facilitator checklists, field notes, and troubleshooting
- Prepare basic descriptive reports, presentations, manuscripts, and other dissemination materials
- Coordinate communication across investigators, sites, and the EAB
- Track recruitment, retention, and adverse events
- Perform other duties and responsibilities as assigned
Requirements
What you’ll need- Bachelor of Science or Bachelor of Arts and 5 to 7 years of experience, or Master of Science or Master of Arts and 2 to 5 years of experience, or equivalent combination of education and experience
- Mental health or clinical research background, such as psychology, nursing, or social work
- Ability to manage regulatory and IRB submissions, amendments, continuing reviews, protocol deviations, and adverse-event documentation
- Knowledge of study protocols and data quality standards
- Experience with participant recruitment, screening, informed consent, enrollment, scheduling, retention, and incentive tracking
- Experience supporting qualitative interviews, transcription review, de-identification, documentation, and qualitative coding
- Experience with human-centered design activities and co-design workshops
- Ability to support pilot RCT procedures and intervention fidelity monitoring
- Ability to prepare descriptive reports, presentations, manuscripts, and dissemination materials
- Background checks may be required after a conditional job offer
Benefits
Comp & perks- Comprehensive medical, prescription, behavioral health, dental, vision, and life insurance benefits
- Flexible spending accounts for eligible health care and dependent care expenses
- Tuition assistance for employees, spouses, and dependent children
- Tuition assistance for dependent children at other institutions
- Basic, Matching, and Supplemental retirement plans
- Pre-tax or Roth retirement savings options
- Investment options through TIAA and Vanguard
- Substantial time away from work, including vacation, personal time, and sick leave
- Long-term care insurance for eligible employees and family members
- Wellness and work-life programs and resources
- Professional and personal development resources
- Access to University libraries, athletic facilities, arboretum, art galleries, museums, and cultural and recreational activities
- Free and discounted admission and memberships at Penn cultural centers and museums
- Discounts on goods and services, including transportation, mortgages, cars, cellular phone plans, movie tickets, and theme parks
- Flexible work options and non-traditional work hours, locations, and/or job structures
- Forgivable home ownership loan for eligible employees in West Philadelphia
- Adoption assistance of qualified expenses for up to two adoptions in the household