Clinical Research Assistant 1 - The Division of Emergency Medicine

Children's Hospital of Philadelphia•Philadelphia, PA

1d•Onsite

About The Position

The Division of Emergency Medicine (DoEM) at Children’s Hospital of Philadelphia (CHOP) is seeking a part-time clinical research assistant to join a highly productive research team. This team focuses on conducting various 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 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. This position will be for evening and weekend hours. CHOP is committed to supporting the health of its patients, families, workforce, and global community, and as a condition of employment, employees who work in patient care buildings or who have patient facing responsibilities must receive an annual influenza vaccine.

Requirements

High School Diploma / GED Required
Previous relevant clinical research experience Required
Familiarity with IRB and human subject protection
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

Nice To Haves

Bachelor's Degree Preferred
At least one (1) year of relevant clinical research experience Preferred

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
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