Clinical Research Assistant I - Division of Emergency Medicine Part Time
About The Position
The Division of Emergency Medicine (DoEM) is seeking a part-time clinical research assistant to join a highly productive research team focused on conducting a variety of research projects at their King of Prussia location. 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 will coordinate 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. Job responsibilities may include human subject research activities including but not limited to subject enrollment, data/sample collection, data entry, and regulatory submissions support.
Requirements
- High School Diploma / GED Required
- Previous relevant clinical research experience Required
- Familiarity with IRB and human subject protection.
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
Benefits
- Annual influenza vaccine
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What This Job Offers
Job Type
Part-time
Career Level
Entry Level
Education Level
High school or GED
