Clinical Trials Research Assistant — NIH Study Support

New York State Psychiatry Institute; New York (NY); On-site; USD 45,000 - 53,000; Full time

Benefits offered by this job

Benefits package

Job summary

The Research Foundation for Mental Hygiene is seeking a full-time Research Assistant to support an NIH-funded study focused on clinical trials. The position requires a highly organized person to manage detailed information in a research environment and assist with study procedures.

The role will involve scheduling subjects, data entry, and assisting Principal Investigators in study administration. Responsibilities include coordinating patient appointments, maintaining databases, helping with IRB

Qualifications

• Bachelor's degree required in health/science related field.
• Experience in clinical settings preferred.

Responsibilities

• Assist in organizing advertising and appointments for, and brief phone screening of potential research subjects
• Organizing databases.
• Help tracking and contacting patients for intake and follow up interviews in research protocols
• Help coordinating patient appointments for psychologists and psychiatrists and assisting psychologists and psychiatrists with research assessments.
• Help preparing data for PI to use in IRB protocol submissions and updates
• Help organizing research charts, creating study chart documents and entering data
• Help monitoring of research charts for completeness and organizing additions and corrections
• Assist in communication with the study supervisor, inpatient unit, and pharmacy as needed
• If applicable, assist in training new hires to assume incumbent responsibilities

Skills

Data entry

Scheduling

Research coordination

Education

Bachelor's degree in health, psychology, medical science or related field

Tools

Databases

Job description

The Research Foundation for Mental Hygiene is seeking a full-time Research Assistant to support an NIH-funded study focused on clinical trials. The position requires a highly organized person to manage detailed information in a research environment and assist with study procedures.

The role will involve scheduling subjects, data entry, and assisting Principal Investigators in study administration. Responsibilities include coordinating patient appointments, maintaining databases, helping with IRB