Blind Assessor

University of Rochester•City of Rochester, NY

1d•$25 - $35•Onsite

About The Position

This position directly conducts and supervises human subjects research from recruitment to follow-up, interacting with research participants, and the supervision of clinical psychology interns in the Crane Lab, URMC Department of Psychiatry. May provide training to new staff members and student employees on federal, state, sponsor and/or institutional regulations, policies and practices related to human subject research. Will be both enrolling participants and conducting a comprehensive psychological evaluation for PTSD and co-occurring conditions. This is a part-time position.

Requirements

Doctoral degree required
2 years of experience required or Equivalent combination of education and experience required
Word processing and data analysis software required

Nice To Haves

Training in the administration of the DIAMOND, CAPS-5, and HAM-D preferred

Responsibilities

Oversees, coordinates and conducts human subject research activities.
Recruits and enrolls participants.
Follows up with study participants regarding assessments and document communications, including protocol deviations.
Completes thorough psychological assessment of PTSD and co-occurring conditions.
Completes some clinical service activities as a component of recruitment, visibility, and familiarity with recruitment site staff and procedures.
Trains new research staff members and student employees on the activities associated with conducting human subject research specific to study protocols and in compliance with Good Clinical Practice (GCPs) guidelines and sponsor requirements.
Directs the activities of student staff members to gather, compile and analyze study information.
Develops, implements and monitors systems and methods to ensure quality, safety, efficiency and consistency in the processing of human subject research data.
Reviews study progress, including data, documentation, and reporting deliverables.
Designs, develops, implements, monitors and manages systems and procedures for the purpose of tracking study progression.
Demonstrates accountability for continuous learning in accordance with Good Clinical Practice guidelines.
Keeps current with industry standards, best practices, and relevant to research studies and designs, implements and monitors resulting study changes.