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Penn Information Systems & Computing

Clinical Research Coordinator

Penn Information Systems & Computing

. Screen, recruit, and enroll study participants .

Posted 10/9/2026full-timePhiladelphia • Pennsylvania • United StatesJunior💰 $47,313 per yearWebsite

Core Competencies

Role fit
Core Competencies

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Demonstrates expertise in recruiting and enrolling study participants while ensuring compliance with FDA and IRB guidelines. Proficient in data management, including entry, coding, and reporting, while promoting good clinical practices in research.

Highest-signal resume keywords
Clinical Study RecruitmentData Entry and ManagementIRB Submission CoordinationKnowledge of FDA GuidelinesHuman Subject Protection

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills
Data CodingData SummarizationStudy Protocol AdministrationClinical InvestigationsRegulatory Compliance
Soft Skills
CommunicationInterpersonal SkillsTeam Collaboration
Certifications & Qualifications
Bachelor of Science
Industry Keywords
Good Clinical PracticeFederal RegulationsHuman Subject ProtectionClinical StudiesStudy Visits

About the role

Key responsibilities & impact
  • Screen, recruit, and enroll study participants
  • Administer study measures during study visits
  • Conduct in-home and on-site study visits
  • Assist with data entry and coding of interviews
  • Prepare data summaries and reports
  • Participate in weekly study progress meetings with the PI and research team
  • Coordinate IRB submissions and renewals
  • Collect, record, and maintain data and source documentation
  • Promote good clinical practice in clinical investigations
  • Talk to participants to determine interest in research
  • Verbally walk participants through consent procedures
  • Administer the study protocol
  • Enter data in the study dataset
  • Distribute study recruitment materials
  • Travel between study visits
  • Perform other duties and responsibilities as assigned

Requirements

What you’ll need
  • Bachelor of Science and 1 to 2 years of experience, or equivalent combination of education and experience, is required
  • In-depth knowledge of federal regulations and guidance documents for clinical studies and human subject protection
  • Knowledge of FDA and IRB guidelines
  • Ability to comply with study protocols and regulatory requirements
  • 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
  • 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 resources, libraries, athletic facilities, arboretum, art galleries, and cultural and recreational activities
  • Free and discounted admission and memberships at Penn arts and cultural centers and museums
  • Discounts on transportation, mortgages, cellular phone service plans, movie tickets, theme parks, and other goods and services
  • Flexible work options and flexible work hours
  • Forgivable homeownership loan for eligible employees
  • Adoption assistance for qualified expenses, up to two adoptions in the household