Clinical Research Assistant -Emergency Medicine

SHIFT:

Evening (United States of America)

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.

The Division of Emergency Medicine (DoEM) is seeking a part‑time (evenings and weekends) clinical research assistant who will join a highly productive research team focused on conducting a variety of research projects at King of Prussia. Researchers in CHOP's DoEM are national leaders in efforts to address important social, biological, and environmental determinants of health for children across the continuum of emergency care – from prevention to recovery.

Under the supervision of the Program Manager and the Associate Director of Research Operations, the research assistant responsibilities include coordinating clinical research activities within the scope of specific research protocols under the guidance of the study PI and Program Manager. The incumbent will assist with recruitment and enrollment of research participants, complete data entry, and follow up with participants as required by the study protocol.

Other tasks may be assigned as needed.

• 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

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

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

• 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

$20.55 - $25.69 Hourly

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.  for more information regarding CHOP's Compensation and Benefits.