Clinical Research Coordinator A
About The Position
This CRC position will support NIH-funded studies focused on improving the implementation of allergy testing and allergen mitigation among adults with persistent asthma. Under the supervision of Dr. Gleeson, the coordinator will assist with preparation of study materials, coordination with clinical sites, screening and recruitment of participants, informed consent, administration of questionnaires, home visits, qualitative interviews, and data entry. The CRC will support participant-facing and operational aspects of the K23 research program, including coordination across clinical settings and maintenance of accurate study documentation. This is a primarily onsite, participant-facing Clinical Research Coordinator position supporting NIH-funded studies focused on improving allergy testing and allergen mitigation among adults with persistent asthma. The CRC will coordinate clinical research activities including study start-up support, participant screening and recruitment, informed consent, scheduling, administration of questionnaires, data collection, data entry, regulatory documentation, and maintenance of accurate study records. The CRC will also support qualitative research activities, including scheduling and conducting semi-structured interviews with patients and providers and organizing audio recordings/transcripts for analysis. The position will coordinate home-visit procedures with study partners, document home environmental assessments and allergen mitigation needs, support delivery of protocolized informational resources, and communicate regularly with the PI, study team, clinical sites, and home-visit collaborators.
Requirements
- Bachelor of Science
- 1 to 2 years of related experience in research and clinical study methodologies or equivalent combination of education and experience
Responsibilities
- Assist with preparation of study materials
- Coordination with clinical sites
- Screening and recruitment of participants
- Informed consent
- Administration of questionnaires
- Home visits
- Qualitative interviews
- Data entry
- Support participant-facing and operational aspects of the K23 research program
- Coordination across clinical settings
- Maintenance of accurate study documentation
- Study start-up support
- Scheduling
- Data collection
- Regulatory documentation
- Conducting semi-structured interviews with patients and providers
- Organizing audio recordings/transcripts for analysis
- Coordinate home-visit procedures with study partners
- Document home environmental assessments and allergen mitigation needs
- Support delivery of protocolized informational resources
- Communicate regularly with the PI, study team, clinical sites, and home-visit collaborators
Benefits
- Excellent healthcare benefits
- Tuition benefits for employees and their families
- Generous retirement benefits
- Wide variety of professional development opportunities
- Supportive work and family benefits
- Wealth of health and wellness programs and resources
- Comprehensive medical, prescription, behavioral health, dental, vision, and life insurance benefits
- Flexible spending accounts for health care and dependent care expenses
- Tuition assistance for employee, spouse, and dependent children
- Tuition assistance for dependent children at other institutions
- Generous retirement plans (Basic, Matching, and Supplemental)
- Pre-tax or Roth retirement savings options
- Wide variety of investment options through TIAA and Vanguard
- Substantial amount of time away from work
- Long-Term Care Insurance
- Wellness and Work-life Resources
- Professional and Personal Development resources
- Access to a wide range of University resources
- Access to cultural and recreational activities
- Discounts and Special Services
- Flexible Work Hours
- Penn Home Ownership Services
- Adoption Assistance
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
