Research Study Coordinator 2


17869 (NE S SEIU 925 Non Supv)
22455 (NE H NI SEIU 925 Non Supv)


Provide professional-level support for clinical, biomedical and/or behavioral science research studies involving human subjects; develop and verify investigative procedures and assist in experimental design.


Under general direction, perform professional level support for research studies involving human subjects. Assist in the design of studies; determine appropriate experimental controls; develop and verify investigative procedures to accomplish research goals; analyze research study results and prepare reports for publication; develop data quality control program.


Assist in the design of studies; review proposals to determine research methods best suited to study objectives;

Establish guidelines for identifying subject populations; develop forms, questionnaires, and clinic procedures for collecting and summarizing observations and data;

Extract technical, medical and/or behavioral information from institution or clinical records;

Record behavior of subjects using sound and video-tape equipment and evaluate effectiveness of data collection;

Determine appropriate psychological/neuropsychological test batteries;
Implement research protocol and monitor participant adherence to protocol; take action to correct problems such as deviation from protocol requirements; verify accuracy of research data;

Assist in developing research proposals;

Dispense and retrieve medication under the direction of a licensed health care practitioner; maintain and monitor drug accountability records;

Review and modify medication schedules as needed in accordance with study protocol and under the direction of a health care practitioner;

Establish and maintain contact with community agencies, health care providers, and/or study sponsors; inform sponsors of current status of research;

Provide referral services to participants;

Assist in modification of procedures for collecting and summarizing data; participate in the development of procedures for the design of measurement instruments and scoring systems;

Use statistical and database management programs to analyze data and prepare summary narrative reports, graphs, tables, charts and illustrations; assist in developing a computerized system for tracking study subjects; monitor data quality control to ensure adherence to study protocol;

Write or review human subjects applications and consent forms in compliance with applicable regulations;

May direct the work of assigned staff;

Perform the duties of Research Study Coordinator I;

Perform related duties as required.


A Bachelor’s degree in a relevant academic area AND two years of experience coordinating the operations of clinical, biomedical, or behavioral research studies involving human subject


equivalent education/experience.


  • New Class: 2-7-92
  • New to CSA: 5-1-00
  • CSR Class Conversion (mc): 06-01-05
  • Revised MQ: 09-08-2023