Research Coordinator 1 (NE S UAW Research)

Job Description

The Division of Metabolism Endocrinology and Nutrition (MET) has an outstanding opportunity for a Research Coordinator 1 position within the Bjornstad Laboratory.

Housed within the UW Medicine Diabetes Institute at the UW South Lake Union campus the Bjornstad laboratory focuses on metabolic and hemodynamic mechanisms underlying the development of diabetic kidney disease (DKD) and cardiovascular disease (CVD) in Type 1 (T1D) and Type 2 (T2D) diabetes and obesity.

The responsibilities of the Research Coordinator (RC) position is to manage the development oversight and execution of research studies of the Bjornstad program. Under the direction of the Research Manager the RC will have minimal supervision in performing assignments. The candidate must be able to work in a fast-paced environment and utilize their resourcefulness independent problem-solving skills excellent time management skills attention to detail and negotiating skills and be adept at communicating priorities about the projects. The RC will work closely with the Principal Investigator Co-Investigators Research Manager other Research Coordinators Regulatory Coordinators collaborators and study stakeholders to execute these various studies.

This position requires operational knowledge of the University of Washington and requires in-depth understanding of the research coordination process and ability to integrate this knowledge with research priorities to implement programmatic goals. The RC will implement study protocol and procedures for several different studies; oversee the clinical research communication system pertaining to recruitment study visits and participant inquiries; and manage the collection of study data and specimens. This position requires the ability to work independently with minimal oversight and the skills to prioritize activities and multi-task to complete multiple scopes of work without benefit of written policies or procedures.

DUTIES AND RESPONSIBILITIES

Research Study Coordination (50%)
Recruit human subjects for research studies independently explaining the purpose of research studies and protocols and obtaining informed consent and enrollment from interested patients.
Creating participant facing forms and databases for studies.
Interpret and apply study protocols.
Monitor study eligibility.
Collect and record clinical data from a combination of electronic medical record systems review and participant study visits.
Maintain and update databases of research subjects.
Identify and help resolve study-related challenges such as recruitment challenges and logistical issues. Use problem solving and interpersonal skills to assist with improvement efforts.
Track study visits and completion of research activities to facilitate protocol adherence billing compliance and to ensure accurate and reliable data collection.
Collect biospecimens (e.g. blood tissue urine) including: processing specimen handling and storage; obtain study laboratory samples and transport obtain biohazard-shipping certification. Remain in compliance with institution and federal regulations.
Prepare reimbursement and donor payments for research subjects upon study completion and maintain financial records.
Assist with other study procedures as needed.

Clinical Participant Communications (20%)
Independently field and respond to clinical study questions or troubleshoot around research activities via email phone and text.
Obtain consent from participants and provide explanation of research studies
Obtain data through interviewing subjects/patients
Send study surveys (monthly) and updates via an electronic mailing list
Schedule participants for study appointments.

Protocol Developments & Study Updates (20%)
Coordinate monthly and quarterly reporting of research activity.
Assist Regulatory Coordinator in preparing Human Subjects Division/Institutional Review Board applications and modifications
Perform routine data quality control measures to ensure study data is accurate and up to date.
Assist in analyzing data to be presented at conferences or published in scientific journals.
Monitor several studies and report findings to principal investigators industry sponsors and Institutional Review Board to ensure that each study is progressing as expected.
Data entry - record and input participant clinical data.
Assist with development of study protocols to ensure appropriate fit with local resources
Create and revise study materials either independently or in collaboration with team members to include case report forms standard operating procedures study operations manuals and other study-related materials as needed.
Aid in the development of research analytical plans that support research data.

External Team Communications & Collaboration (10%)
Participate and represent UW in study-related meetings and conference calls related to multiple studies.
Respond to inquiries from UW and external investigators regarding recruitment status study timelines and research protocols.
Collaborate with teams and individuals conducting related work in collaborating departments/Institutes such as KRI and the UWMDI Clinical Research Unit.

Participate in writing study manuscripts.

MINIMUM REQUIREMENTS

• Bachelors degree in a related field and one year of relevant experience in an academic research environment clinical research laboratory research project coordination research data collection related to human health.

Equivalent education and/or experience may substitute for minimum qualifications except when there are legal requirements such as a license certification and/or registration.

ADDITIONAL REQUIREMENTS
Prior experience in an academic research environment clinical research laboratory research project coordination research data collection related to human health.
Knowledge of research involving human subjects implementation and analysis excellent written and verbal communication skills.
Able to work independently self-starter take on a leadership role whilst also being a team player; to maintain positive vision sense of humor and flexibility; to multi-task as priorities change maintaining a professional demeanor at all times.
Strong organizational skills and attention to detail ability to multitask with competing priorities independent problem-solving skills and excellent time-management skills.

DESIRED QUALIFICATIONS

Experience or knowledge working in a clinical setting.
Certification in Good Clinical Practice.
Human subjects ethics training.
DMID source document and regulatory document training HIPAA and other clinical research training.
Experience with EPIC/ORCA/MINDSCAPE/MAX/LIS record systems.

CONDITIONS OF EMPLOYMENT

Office and participant visit location in the UW Diabetes Institute F Building.
May require climbing stairs to access office location.
Must have flexibility to meet programmatic needs by adjusting work schedule.
Ability to travel to meetings off site.

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Compensation Benefits and Position Details

Pay Range Minimum:

Pay Range Maximum:

Other Compensation:

Benefits:

Temporary or Regular

FTE (Full-Time Equivalent):

Union/Bargaining Unit:

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 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 or .

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.