Research Coordinator 1

University of Washington

Seattle, WA

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JOB DETAILS

SKILLS

Analysis Skills, Billing, Budgeting, Calendar Management, Case Report Form (CRF), Cerebral Vascular Accident, Clinical Practices/Protocols, Clinical Research, Clinical Trial, Compensation and Benefits, Conferences, Corrective Action, Data Analysis, Data Collection, Data Management, Data Quality, Design Document, Diversity, Editing, FDA (Food and Drug Administration), FDA Requirements, Financial Audit, Financial Disclosure, GCP (Good Clinical Practices), IRB/IEC (Institutional Review Board/Independent Ethics Committee), Informed Consent, Maintain Compliance, Medical Billing, Medical Treatment, National Institutes of Health (NIH), Neurology, Organizational Skills, Patient Follow-up, Patient Registration, Patient Safety, Presentation/Verbal Skills, Private Funding, Procedure Development, Procedure Implementation, Project/Program Management, Publications, Regulations, Regulatory Compliance, Regulatory Requirements, Reporting Skills, Research Skills, Scientific Publications, State Laws and Regulations, Team Player, Testing, Time Management, Writing Skills

LOCATION

Seattle, WA

POSTED

30+ days ago

**Job Description** **The Department of Neurology** **has an outstanding opportunity for** **100% FTE Research Coordinator 1.** **About This Opportunity** Reporting to the Principal Investigator the Research Coordinator will be responsible for the coordination and implementation of research projects that focus on the understanding, treatment, and outcomes of stroke. This individual will develop and review research tools and protocols, maintain IRB approvals and consent forms, and participate in data collection and data management for NIH and industry sponsored projects. Additional duties may include, but are not limited to, coordinating multiple data collection efforts with other institutions, designing the phases of the research projects, recruiting and overseeing recruitment of human subjects, writing and editing reports, data management, and preparing conference presentations and manuscripts for publication. This position requires the ability to integrate information from multiple sources to ensure that all research proposals meet the requirements of the University, the Food and Drug Administration, the National Institutes of Health and the study sponsor. This individual will develop procedures that ensure that all research meets or exceeds these requirements. There are multiple resources available within the University system (e.g. Grant and Contract Services, Institutional Review Board, Office of Industry Relations) to help in this process, but ultimately, the work must be done independently and in a resourceful manner to expedite the research objectives. This individual is also responsible for organizing and facilitating sponsor-initiated, FDA-initiated, and institution-initiated audits of study data. They will also be responsible for maintaining communication with researchers at other universities. The individual in this position will aid in furthering the academic pursuit of the UW by contributing their time and knowledge base to our research studies. **Key Responsibilities** **_Patient Management - 50%_** + Identify, consent, enroll and follow up patients in clinical trials. Assist in scheduling appointments, ordering tests and procedures to facilitate protocol adherence, billing compliance, and to ensure accurate and reliable data collection. Assist in monitoring and administering patient protocol, interacting closely with clinical providers to ensure patient safety and protocol adherence. + Communicate with outside physicians who are interested in referring patients to UWMC/HMC for clinical trials in stroke. + Understand clinical trial budget and billing plan for patients enrolled on clinical trials. Work with internal partners to ensure clinical trials are performed in accordance with institutional requirements for billing compliance. Assist in financial audits as necessary. Communicate with investigators and research staff when financial milestones have been met. **_Protocol Management - 40%_** + Develop and implement research project procedures that meet research objectives and ensure compliance with all aspects of Institution, Federal Drug Administration (FDA) and National Institutes of Health (NIH) regulations pertaining to clinical research in human subjects (e.g. investigator financial disclosure requirements of the FDA). + Design, create, revise, and complete research instruments (e.g. case report forms) as necessary to ensure quality data that correlates with research objectives. + Design, develop, document and maintain policies and procedures for patient registration and protocol implementation to ensure that research execution meets Good Clinical Practice guidelines. Design, create and revise research instruments (e.g. case report forms) as necessary to ensure quality data that satisfies research objectives. Design, document and implement procedures for audits to assure protocol compliance and to ensure research data quality. Develop and implement corrective action plans to ensure protocol adherence and data integrity. + Ensure that projects are executed successfully and completed within required time frames to meet research objectives. **_Analysis and Reporting - 10%_** + Prepare interim reports for principal investigators, industry sponsors and Institutional Review Board to ensure that each project is moving toward timely completion. Assist in analyzing data to be presented at conferences or published in scientific journals. + Assist in financial audits and communicate with research investigators when financial milestones have been met. + Prepare interim reports for the research program and sponsors to ensure that each project is moving toward timely completion. Other duties as assigned. **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** + Bachelor's degree in a related field and one year of relevant experience. + Equivalent education and/or experience may substitute for minimum qualifications except when there are legal requirements, such as a license, certification, and/or registration. + **Applicants who do not meet these qualifications WILL NOT be forwarded to the Hiring Manager.** **Additional Qualifications** + Knowledge and prior experience with human subject's institutional review process including developing protocols and working with the IRB for approvals. + Strong writing skills including a demonstrated ability to write for publication in peer-reviewed scientific journals. + Strong project management skills. + Background and experience conducting research projects that met programmatic and regulatory requirements. + Training and/or knowledge in ethical conduct of research with human subjects. + Ability to work as a collaborative, cooperative, and congenial member of a close knit scholarly and administrative team, as well as work independently. **Preferred Qualifications** + Certifications in Health Information Portability and Accountability Act and Human Subject Research. **Compensation, Benefits and Position Details** **Pay Range Minimum:** $55,944.00 annual **Pay Range Maximum:** $64,992.00 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:** UAW Research **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 (https://policy.uw.edu/directory/po/executive-orders/eo-81-prohibiting-discrimination-harassment-and-sexual-misconduct/) . 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 (https://app.leg.wa.gov/RCW/default.aspx?cite=28B.112.080) . University of Washington is an affirmative action and equal opportunity employer. All qualified applicants will receive consideration for employment without regard to, among other things, race, religion, color, national origin, sexual orientation, gender identity, sex, age, protected veteran or disabled status, or genetic information.

About the Company

University of Washington

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