Clinical Research Assistant I - The Center for Injury Research and Prevention (CIRP)

SHIFT:

Seeking Breakthrough Makers

Children’s Hospital of Philadelphia (CHOP) offers countless ways to change lives. Our diverse community of more than 20,000 Breakthrough Makers will inspire you to pursue passions, develop expertise, and drive innovation.

At CHOP, your experience is valued; your voice is heard; and your contributions make a difference for patients and families. Join us as we build on our promise to advance pediatric care—and your career.



CHOP does not discriminate on the basis of race, color, sex, national origin, religion, or any other legally protected categories in any employment, training, or vendor decisions or programs. CHOP recognizes the critical importance of a workforce rich in varied backgrounds and experiences and engages in ongoing efforts to achieve that through equally varied and non-discriminatory means.


A Brief Overview

The Center for Injury Research and Prevention (CIRP) at The Children’s Hospital of Philadelphia (CHOP) is seeking a part-time Research Assistant I (RA I) to support the Neuroscience of Driving (NoD) Program. The Research Assistant will support an interdisciplinary research team working primarily on a large, NIH-funded randomized controlled trial studying how teens learn to drive and testing novel interventions to improve driver safety.

This is a part-time position requiring approximately 20–25 hours per week. The
Research Assistant will serve as one of the primary points of contact for study
participants and families and will support day-to-day study operations through
participant recruitment, scheduling, consenting, study visit support, and administrative tasks. The RA I will work closely with the Clinical Research Study Lead, Principal Investigator, and other study staff to support the operational needs of the research team.

Some evening and weekend hours are required to accommodate participant availability,including conducting recruitment and consent phone calls and facilitating study visits. Evening shifts will typically occur between 3:00 p.m. – 7:00 p.m. or 4:00 p.m. – 8:00 p.m., depending on study scheduling needs. Saturday shifts may also be required and will typically occur between 9:00 a.m. – 3:00 p.m.

Depending on study needs, the individual in this position may work 1–3 days per week conducting offsite study visits at CHOP Primary Care Sites or other approved community locations. Applicants must be willing and able to travel to offsite study locations to support recruitment and study operations. Local travel to CHOP Primary Care Sites, the study’s partner driving school, and other approved community locations may be required. Applicants with a valid driver’s license and access to a personal vehicle are strongly encouraged to apply.

This position is grant-funded and continuation is contingent upon funding availability and programmatic needs.

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.

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 receive an annual influenza vaccine. Learn more.

EEO / VEVRAA Federal Contractor | Tobacco Statement

SALARY RANGE:

Salary ranges are shown for full-time jobs. If you're working part-time, your pay will be adjusted accordingly.

-------------------

At CHOP, we are committed to fair and transparent pay practices. Factors such as skills and experience could result in an offer above the salary range noted in this job posting. Click here for more information regarding CHOP's Compensation and Benefits.