Research Study Coordinator I - Cancer Clinical & Trans Research - 40 hours - Days

About the Role

Under minimal supervision, coordinates research projects within guidelines of regulatory compliance and/or Code of Federal Regulation. Provides technical support to Principal Investigators.

Duties include interacting with both internal and external customers at all levels, oversight of recruitment, and coordinating day-to-day operations of the study. Direct contact with potential and enrolled study participants is expected. Provides other support as required.

Responsibilities

• Coordinate research projects in compliance with regulatory guidelines and Code of Federal Regulation.
• Provide technical support to Principal Investigators.
• Interact with internal and external customers at all levels.
• Oversee recruitment and coordinate day-to-day study operations.
• Maintain direct contact with potential and enrolled study participants.
• Provide additional support as required.

Requirements

• Bachelor’s degree in a scientific field, Psychology, Sociology, Anthropology, or a related field.
• SOCRA or ACRP certification and IATA certification preferred.
• Reliable transportation to drive to various locations.

Preferred Skills

• Research experience.
• Good communication skills.
• Clinical skills, including phlebotomy (useful but not required).