Job Description

Responsibilities:

• This role participates in the recruitment and screening activities to ensure successful enrolment of volunteers into studies scheduled at the Phase 1 Unit.
• Interfaces with research participants, to support efforts to determine eligibility and consenting of study participants according to protocol (R/S).
• The role interacts with the Principal Investigator and other study physicians, Recruiting/Screening department, Data Systems, and other personnel in support of study-specific activities.

Top Skills:

• Fundamental working knowledge of clinical research.
• ble to review study protocols and educate study participants as part of the consent process.
• bility to organize and prioritize responsibilities while paying close attention to detail.
• ble to work in a team-driven environment.

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