Research Coord RN-Oncology Research

Summary:
Coordinates research projects, with applicable research management systems, processes, and monitors progress and completion of clinical studies/trials.

Work Schedule: Full Time Days

Responsibilities:
Maintains required documentation of study activity including pending orders, case report forms, drug dispensation records, and/or regulatory forms and any other relevant documentation.

Conducts informed consent, provides clinical education, performs clinical procedures and other clinical assessments on study participants per the protocol and within scope of practice. Assists with the pre-screening, selection, education, testing and monitoring of research participants.

Prepares study-related documentation such as protocol worksheets, procedural manuals, adverse event reports, institutional review board documents, and progress reports. Assists with the preparation, submission and management of internal/external compliance documentation at all stages of the research project.

Maintain contact with sponsors and research colleagues to schedule and coordinate site visits or to answer questions about issues such as incomplete data.

Withinscope of job, requires critical thinking skills, decisive judgement and theability to work with minimal supervision. Must be able to work in afast-paced environment and take appropriate action.