RESEARCH STUDY COORDINATOR 1

Job Description

The Diabetes Institute Clinical Research Unit (CRU) has an outstanding opportunity for a full time RESEARCH STUDY COORDINATOR.

About this Opportunity

This position will report to the CRU Research Coordinator Supervisor, and is responsible for developing and maintaining ongoing support for clinical studies within the unit. Under the supervision of the nurse manager and the medical director, the research coordinator will follow research protocols to obtain data through interviewing subjects/patients, conducting laboratory tests, following research protocols, coordinate patient participation in medical research studies and compile and verify the accuracy of research data.

Key Responsibilities

Research Study Management:

• Under general supervision, coordinate the operations of clinical, biomedical, and/or behavioral research studies involving human subjects
• Coordinate specialized tasks with the research team such as the operation of equipment, processing of laboratory specimens, administering of treatment and/or medication in accordance with research protocol, assessment of patient reaction to medications and/or treatments as part of a research protocol and identification of potential adverse reactions

• Perform certain non-invasive patient oriented procedures

• Responsible for the processing and shipping of study-specific laboratory specimens

• Coordinate physician examinations and study protocol for technicians

• Assist in planning aspects of team research

• Keep study files in compliance with Food and Drug Administration's regulations

• Read, interpret and communicate protocol for clinical studies providing data on the safety and efficacy of new drugs

• Establish and maintain effective working relationships with patients and their families, professional or community groups and volunteers

• Maintain contact with Principal Investigators, Co-Investigators, and public agencies which are involved with aspects of the research

Research Data Management:

• Maintain records of study data.

• Design data collection tools.

• Obtain and record research data in conjunction with physician and other professionals on the research team.

• Assist in preparing interim reports for Principal Investigators, Study Sponsor and Human Subjects Review Board to ensure that each project timeline is being met.

• Communicate with Principal Investigators, pharmaceutical and equipment company medical personnel in handling results of studies (progress reports, case report forms).

Patient/Participant Management:

• Screen, recruit and interview potential subjects to determine eligibility according to specific study protocols

• Obtain informed consent

• Enroll patients in research protocol

• Explain research protocol to participants

• Respond to patient inquiries regarding protocol

• Schedule patient participation

• Coordinate all aspects of the patient's care

• Ensure compliance with research protocol

• Inform referring physicians of protocol requirements

• Perform other duties as required

Required Qualifications

To be considered for this opportunity your application must demonstrate you meet both the minimum qualifications and additional qualifications listed below. Equivalent education and/or experience may substitute for minimum qualifications except when there are legal requirements, such as a license, certification, and/or registration.

Minimum Qualifications

• Two years of college level course work in a relevant academic area AND two years of experience as a Research Study Assistant or equivalent education/experience.

Applicants who do not meet these qualifications WILL NOT be forwarded to the Hiring Manager.

Preferred Qualifications

• Ability to multi-task
• Excellent verbal and written communication skills

• Experience with clinical research coordination, including interviewing subjects, developing protocols, and providing support to the medical team

• Experience with diabetes and related disorders

• Experience with database management and a working knowledge of MS Excel
• Experience with the UW grant approval process

• Experience with clinical trials

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Compensation, Benefits and Position Details

Pay Range Minimum:

$45,288.00 annual

Pay Range Maximum:

$56,124.00 annual

Other Compensation:

Benefits:

For information about benefits for this position, visit https://www.washington.edu/jobs/benefits-for-uw-staff/

Shift:

First Shift (United States of America)

Temporary or Regular?

This is a regular position

FTE (Full-Time Equivalent):

100.00%

Union/Bargaining Unit:

SEIU Local 925 Nonsupervisory

About the UW

Working at the University of Washington provides a unique opportunity to change lives – on our campuses, in our state and around the world.

UW employees bring their boundless energy, creative problem-solving skills and dedication to building stronger minds and a healthier world. In return, they enjoy outstanding benefits, opportunities for professional growth and the chance to work in an environment known for its diversity, intellectual excitement, artistic pursuits and natural beauty.

Our Commitment

The University of Washington is committed to fostering an inclusive, respectful and welcoming community for all. As an equal opportunity employer, the University considers applicants for employment without regard to race, color, creed, religion, national origin, citizenship, sex, pregnancy, age, marital status, sexual orientation, gender identity or expression, genetic information, disability, or veteran status consistent with UW Executive Order No. 81 .

To request disability accommodation in the application process, contact the Disability Services Office at 206-543-6450 or dso@uw.edu .

Applicants considered for this position will be required to disclose if they are the subject of any substantiated findings or current investigations related to sexual misconduct at their current employment and past employment. Disclosure is required under Washington state law .