Clinical Research Assistant I-Emergency Medicine

Children's Hospital of Philadelphia•King Of Prussia, PA

32d•$21 - $26

About The Position

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.

Requirements

High School Diploma / GED - Required
Previous relevant clinical research experience - Required

Nice To Haves

Bachelor's Degree - Preferred
At least one (1) year of relevant clinical research experience - Preferred
Familiarity with IRB and human subject protection.

Responsibilities

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
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