SHIFT:
Evening (United States of America)The Center for Injury Research and Prevention (CIRP) is seeking a Part-Time Research Assistant to support translational research in concussion care. An in-person schedule with the ability to travel locally between ED clinic and community sites on weekends and/or weekday afternoons to evening hours (times negotiable) to leverage research recruitment success across projects. This individual will provide operational support to research projects within the Minds Matter Concussion Program. Responsibilities will include but not be limited to data collection, data entry, medical record abstraction, study enrollment activities and study procedures. 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.
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We strongly encourage all candidates of diverse backgrounds and lived experiences to apply.
A Brief Overview
Under the direct supervision of the Principal Investigator and/or other study team members, this role provides support in the conduct of clinical research.
Job responsibilities may include human subject research activities including but not limited to subject enrollment, data/sample collection, data entry, and regulatory submissions support.
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. (Required proficiency)
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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