Overview:

GENERAL SUMMARY OF POSITION:

Under the direction of the Principal Investigator or designee, the Research Coordinator II is responsible for independently carrying out multiple complex and diverse research initiatives. 

Responsibilities:

MAJOR RESPONSIBILITIES:

Provide support to projects through implementation of work plans, and preparation of deliverables.  Assist in the documentation of project writing, preparation of material for project meetings and IRB submissions, summary reports, ongoing project evaluations, and coordinate arrangements applicable to assigned projects such as interview arrangements, etc.

Administratively responsible for the clinical aspects of patient study subjects and testing 

Participate in preparing project-specific data collection efforts including surveys, interviews, focus groups involving patients, state agency personnel and other key informants. Record and analyze pertinent data. Evaluate and update data in relation to protocol

Design and execute protocols and experiments, modify protocols as needed, and may be responsible for own research project

Oversee development of data collection instruments, survey tools and interview guides, perform and oversee data collection, management and analysis as necessary

Assist in writing the text of scientific publications and grants.  Review literature

Assist in design, development and implementation of research endeavors for multiple principal investigators

Assist with the budget/operational aspects of the revenue and expense accounts. Compile expenses for fiscal reports and grant budgets. Assist grant accounting with grant reporting requirements.

Responsible for maintaining all regulatory paperwork from study initiation, continuation, and termination (includes application for IRB, informed consents, HIPAA Authorization, etc.)

May help recruit, select, supervise and direct the activities of data collection employees, Research Technicians, and Research Coordinators

Comply with all safety and infection control standards appropriate to this position

Responsible for the inventory of research related supplies.

Perform other duties as required.

Qualifications:

REQUIRED QUALIFICATIONS:

Bachelor’s degree in a scientific or health care field, or equivalent experience

3 years of related experience

Demonstratedknowledge of federal requirements for the conduct of clinical trials

Experience in using computer based tools (Word, Excel, Access, Outlook, PowerPoint, etc.)

Oral and written communication skills

Excellent organization, analytical, and interpersonal skills required

Ability to travel to off-site locations

                                                                                               

SUPERVISION RECEIVED:

Under the general supervision of the Principle Investigator or designee

SUPERVISION EXERCISED:

Supervise and direct the activities of data collection employees, lab technicians & research coordinator I’s

ENVIRONMENTAL WORKING CONDITIONS:

Usual office environment, laboratory, medical, surgical, and off campus study sites

Additional Information:

Additional Information and Preferred Qualifications

This position involves research-related tasks for federally and state funded research projects in the Law & Psychiatry Program at the Implementation Science and Practice Advances Research Center (iSPARC). Research activities will include, but not be limited to, quantitative and qualitative data coding, data management and analyses, attending meetings and recording focus groups with partners and individuals with lived experience from various legal settings, and rigorous literature reviews and summaries.

Advanced SPSS skills preferred