Clinical Research Assistant I

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We strongly encourage all candidates of diverse backgrounds and lived experiences to apply.

A Brief Overview

The Center for Injury Research and Prevention (CIRP) is seeking a full-time Research Assistant to support translational research in concussion care. A flexible in-person schedule with the ability to travel locally will be needed to leverage research recruitment success across clinic settings and community partners. Under the direct supervision of the Program Manager, this individual will provide administrative and operational support to research projects within the Minds Matter Concussion Research Program. Responsibilities will include but not be limited to data collection, data entry, medical record abstraction, study enrollment activities, administrative research support, and participation in team meetings. As a Research Assistant for the Minds Matter Concussion Program, training will be provided to support a strong aptitude for learning and future growth through professional development opportunities.

Primarily based out of King of Prussia, this role requires visits to our Philadelphia locations on a weekly basis.

What you will do

• Provide technical and administrative support in the conduct of clinical research:
• Patient/research participant scheduling
• Patient/Research Participant screening for inclusion/exclusion criteria or case history
• Data collection
• Data entry
• Data management
• Laboratory sample processing
• Clinical research study procedures or questionnaire administration
• Organization of research records and/or other study related documentation
• Research Study Compliance
• Adhere to IRB approved protocols and compliance with HIPAA and handling confidential materials
• Comply with Institutional policies, SOPs and guidelines
• Comply with federal, state, and sponsor policies
• Additional Responsibilities may include:
• Consent subjects, with appropriate authorization and training
• Document and report adverse events
• Maintain study source documents
• Complete case report forms (paper and electronic data capture)
• Assist with IRB/regulatory submissions
• Complete case report forms or other study documentation (paper and electronic data capture)
• Follow-up care
• Order materials/supplies
• Schedule research meetings

Education Qualifications

• High School Diploma / GED Required
• Bachelor's Degree Preferred

Experience Qualifications

• Previous relevant clinical research experience Required
• At least one (1) year of relevant clinical research experience Preferred

Skills and Abilities

• Familiarity with IRB and human subject protection.

To carry out its mission, CHOP is committed to supporting the health of our patients, families, workforce, and global community. As a condition of employment, CHOP employees who work in patient care buildings or who have patient facing responsibilities must be fully vaccinated against COVID-19 and receive an annual influenza vaccine. Learn more.

Employees may request exemptions for valid religious and medical reasons. Start dates may be delayed until candidates are immunized or exemption requests are reviewed.

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