Reference #: 1012765
SHIFT:Day (United States of America)A Brief Overview
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 meetingsEducationRequired: Associate degreePreferred: Bachelor's degreeExperienceRequired: At least two (2) years relevant clinical research experienceSkills and AbilitiesBasic knowledge of IRB and human subject protectionChildren's Hospital of Philadelphia is an equal opportunity employer. We do not discriminate on the basis of race, color, gender, gender identity, sexual orientation, age, religion, national or ethnic origin, disability or protected veteran status.
