Research Study Assistant II - 40 Hours - Days

This role is ideal for individuals with previous experience in medicine, including backgrounds as a medical scribe, nurse, medical assistant, or clinical research professional. The Research Study Assistant plays a key role in supporting clinical research operations, ensuring regulatory compliance, and engaging directly with study participants. Candidates should be detail-oriented, comfortable in both patient-facing and administrative tasks, and eager to contribute to meaningful research efforts.

GENERAL SUMMARY:

Under limited supervision, the Research Study Assistants responsible for:

Carrying out research projects within guides of regulatory compliance and/or Code of Federal Regulation. Duties include but are not limited to interacting with both internal and external customers at all levels and completing day to day operational tasks for the study. Direct contact with potential and enrolled study participants expected. May analyze protocol specific requirements and implement measures to ensure stakeholder compliance. Provides other support as required.