Research Coordinator 4 (E S UAW Research)

University of Washington•Seattle, WA

22h•Onsite

About The Position

The Department of Ophthalmology has an outstanding opportunity for Research Coordinator 4 to join their team. OVERVIEW : Reporting to the Associate Director of Research, the Research Coordinator 4 serves as the subject matter expert on the full scope of clinical research education, management and compliance for the entire Department of Ophthalmology at the University of Washington. The Research Coordinator 4 with collaborate with the Associate Director of Research to oversee educational programs that span the entire scope of clinical research operations, including training, trial start-up, study management, regulatory compliance, financial operations, and billing practices. The Research Coordinator 4 provides strategic leadership, oversight, and operational management of regulatory affairs and research compliance activities supporting clinical research programs at the University of Washington (UW). This position ensures that all clinical research activities are conducted in accordance with federal, state, local, sponsor, and institutional requirements, including regulations governing human subjects research, FDA-regulated studies, Good Clinical Practice (GCP), and institutional review board (IRB) oversight. The Research Coordinator 4 serves as the department's subject matter expert in clinical research regulation, compliance, education, and operations, partnering with investigators, study teams, sponsors, and institutional stakeholders to ensure research excellence and regulatory compliance. The Research Coordinator 4 provides strategic leadership for regulatory affairs and research compliance programs, including regulatory submissions, compliance monitoring, personnel supervision, and corrective action initiatives supporting clinical research across the Department of Ophthalmology.

Requirements

Master’s degree in Clinical Research Administration, Health Care Administration, Regulatory Science, or a related field.
Four (4) years of progressively responsible experience in clinical research, regulatory affairs, research compliance, or related healthcare environment.
Advanced knowledge of FDA, GCP, NIH, OHRP, HIPAA and other applicable clinical research regulations.
Demonstrated experience managing regulatory submissions, research compliance programs, audits, inspections, and regulatory documentation.
Experience supporting investigator-initiated studies and FDA IND/IDE submissions.
Experience developing and delivering research education and training programs.
Experience using electronic IRB systems, CTMS platforms, and other research regulatory systems.
Demonstrated leadership, project management, and personnel supervision experience.
Excellent written, verbal, and interpersonal communication skills.
Demonstrated ability to exercise independent judgment, manage multiple priorities, and handle confidential information with discretion.
Proficiency with: - Microsoft Office Suite - Electronic IRB systems - Clinical Trial Management Systems (CTMS) - Electronic regulatory platform

Nice To Haves

At least 5 years of management experience working in an academic medical center or a clinical research organization.
Professional certification such as: - Certified Clinical Research Professional (CCRP) - Certified Clinical Research Coordinator (CCRC)

Responsibilities

Independently coordinate and oversee regulatory and compliance activities for complex investigator-initiated and/or industry-sponsored clinical research studies, exercising professional judgment in interpreting institutional, federal, and sponsor requirements.
Manage regulatory submissions including: - Initial IRB applications - Continuing reviews - Modifications and amendments - Reportable events - Safety reports - Study closures
Maintain complete and audit-ready regulatory documentation, including TMFs and records within OnCore and other regulatory systems.
Develop and disseminate standardized tools, templates, and job aids to support all operational phases of clinical research from start-up to close-out.
Obtain and maintain IRB approvals, including initial submissions, continuing review, protocol modifications, amendments, and study closures.
Report and document safety issues (e.g. adverse events) to the applicable oversight body.
Prepare for and participate in sponsor audits and/or regulatory inspections, if applicable.
FDA Investigational New Drug and Device Exemption (IND/IDE) application support.
Serve as the primary regulatory liaison for investigators, study teams, sponsors, and oversight bodies.
Coordinate and support the development, implementation, and continuous improvement of research compliance processes and programs supporting clinical trials and human subjects research.
Develop, implement, and maintain research compliance programs supporting clinical trials and human subjects research.
Evaluate study activities for adherence to: - FDA regulations - OHRP requirements - HIPAA regulations - Good Clinical Practice (ICH-GCP) - University of Washington policies - Sponsor requirements
Track compliance metrics and prepare reports for departmental and institutional leadership.
Lead compliance monitoring, risk assessments, audits (sponsor, FDA, NIH, OHRP, institutional), and inspection-readiness activities; manage findings, CAPA plans, and reporting to ensure ongoing adherence to regulatory and institutional requirements.
Collaborate with investigators and study teams on protocol development, study start-up activities, and preparation of related study documentation.
Review protocols, informed consent documents, and ancillary materials for regulatory compliance.
Assist in developing standard operating procedures (SOPs) and work instructions.
Support study initiation, monitoring visits, sponsor audits, and regulatory inspections.
Design, oversee, and deliver role-based clinical research training programs for faculty and staff, ensuring alignment with institutional, sponsor, and regulatory requirements.
Develop and maintain training matrices, tracking systems, competency assessments, and needs analyses to monitor compliance and workforce development.
Ensure training reflects current FDA, cGCP, cGMP, NIH, CMS billing rules, and institutional guidelines.
Communicate timely regulatory changes and operational updates to research teams through multiple channels, including presentations, workshops, and reference materials.
Foster a culture of accountability, quality, compliance, and continuous improvement through staff development, process optimization, and adoption of best practices.
Participate in institutional committees and working groups.
Contribute to strategic planning efforts supporting UW clinical research programs.
Supervise regulatory specialists, compliance coordinators, research coordinators and related research support staff.
Serve as a resource and mentor for study team regarding regulatory best practices.
Collaborate with the UW regulatory offices, research administration, and external partners to leverage resources and share best practices.
Other duties as assigned.