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

GENERAL SUMMARY:

• Under minimal supervision, coordinates research projects within guides of regulatory compliance and/or Code of Federal Regulation.
• Provides technical support to Principal Investigators.
• Duties include but not limited to, interacting with both internal and external customers at all levels and oversight of recruitment and coordinating day-to-day operations of the study.
• Direct contact with potential and enrolled study participants expected.
• Provides other support as required.

EDUCATION/EXPERIENCE REQUIRED:

• Bachelor's degree in a scientific field, Psychology, Sociology, Anthropology or related field.
• CERTIFICATIONS/LI
• CENSURES REQUIRED: SOCRA or ACRP and IATA certification preferred.
• Preferred Skills
• Research Experience
• Good Communication skills
• Reliable transportation to drive to various locations,
• Clinical skills including phlebotomy could be extremely useful but not required.