Clinical Research Coordinator II Addictions Psychiatry

The Clinical Research Coordinator II (CRC II) will assume the responsibility for overall study coordination for research conducted within the Division of Addiction Psychiatry and its collaborators. The CRC will coordinate clinical research, including but not limited to: assisting with recruitment efforts overall; administering screening instruments, interviews, and surveys; conducting, scheduling, and managing study visits; obtaining consent; managing data; preparing documents for, ensuring compliance with, and corresponding with the Institutional Review Board (IRB) and other regulatory groups such as the FDA and DEA; assisting with preparation of manuscripts, protocols, and grants; performing data entry and analysis; and completing other projects in collaboration with principal investigator(s) and collaborators. The CRC II must be able to interact respectfully with all study participants.

A bachelor's degree is required, with minimum 1 year directly related post Bachelor's degree experience working in clinical research, academic research or similar environment required.

Exposure to IRB preparation, interactions with CROs, site monitors, regulatory paperwork regulatory paperwork, consenting and interacting with study subjects, strict protocol adherence and archiving is preferred.

Familiarity with working in a large healthcare organization/ academic center encouraged.