PS Study Coordinator

Responsibilities:

Essential Functions

1. Coordinates and performs responsibilities such as patient identification, recruitment, and offering enrollment in the Total Cancer Care study.
2. Offer questionnaires to enrolled study participants regularly at the time of consent or via follow-up contact.
3. Maintains information in patient databases and is responsible for data entry.
4. Recognizes and informs study team of protocol deviations and participates in documentation of deviations.
5. Assists the Total Cancer Care Program Manager and Associate Director with research and team related tasks.
6. Works closely with the Biorepository and Molecular Pathology Shared Resource and investigators and ensures proper collection and processing of specimens.
7. Is responsible to arrange coverage when not present.
8. Performs other responsibilities as required.

Problem Solving

S/he prioritizes and helps optimize processes needed to achieve study goals. S/he functions independently under minimal supervision. S/he has an understanding of good clinical practice and research processes.

Bachelor’s degree in a related field, or equivalency (one year of education can be substituted for two years of related work experience) required. IRB CITI Course in the Protection of Human Research subjects certificate obtained within six months of hire Bachelor’s degree in a related field, or equivalency (one year of education can be substituted for two years of related work experience) required. IRB CITI Course in the Protection of Human Research subjects certificate obtained within six months of hire and demonstrated human relations and effective communication skills are also required.