Research Coordinator 2 (NE S UAW Research)

UW Medicine; Seattle, Northern (WA, KY); Hybrid; USD 65,000 - 120,000; Full time

Job summary

UW Medicine's Department of Emergency Medicine in Seattle seeks a Research Coordinator 2 to oversee day-to-day operations of a large pragmatic multi-center randomized trial across 17 U.S. hospital sites, primarily Harborview Medical Center.

The RC2 will manage study start-up, site activation, enrollment tracking, and training materials while ensuring regulatory compliance. Candidates should have at least 2 years coordinating multi-center trials, experience with REDCap, and familiarity with FDA

Qualifications

• Minimum 2 years coordinating multi-site clinical trials in emergency care or similar setting.
• Experience with REDCap or other electronic data capture systems.
• Strong organizational and communication skills with ability to manage priorities.

Responsibilities

• Oversee day-to-day multi-site trial operations across 17 enrolling centers.
• Coordinate start-up, activation, enrollment tracking, and site communication.
• Monitor protocol adherence and data quality; resolve deviations.
• Prepare regulatory submissions and reports for oversight committees.
• Support training materials, site training, and onboarding of site coordinators.
• Ensure compliance with GCP, HIPAA, FDA regulations.

Skills

REDCap

Data management

Regulatory compliance

Multi-site coordination

Education

Bachelor’s degree in related field

Tools

REDCap

Microsoft Office Suite

Job description

**Job Description****The Department of Emergency Medicine has an outstanding opportunity for a Research Coordinator (Research Coordinator 2 (NE S UAW Research)) to join their team.** **OVERVIEW:**The department of Emergency Medicine is seeking an experienced RC2 to serve as the primary coordinator overseeing day-to-day operations of a large pragmatic multi-center randomized controlled trial. Reporting to the Clinical Research Operations Manager and working closely with Principal Investigators, the RC2 will support the VICTORY and VICTORY-CART trials, which compare vasopressor strategies for post-cardiac arrest shock across 17 U.S. hospital sites.The RC2 will oversee all aspects of trial coordination including development and maintenance of study protocols, standard operating procedures, and training materials; onboarding and ongoing support of site coordinators and clinical teams at all 17 enrolling centers; real-time monitoring of enrollment, protocol adherence, and data quality across sites using REDCap and automated reporting tools; coordination of regulatory submissions and amendments with the BRANY single IRB; preparation of reports for the Data and Safety Monitoring Board, PCORI, and the Steering Committee; and identification and resolution of protocol deviations, crossover events, and site-level barriers to enrollment. The ideal candidate will have a minimum of 2 years of experience coordinating multi-center clinical trials, demonstrated experience managing remote site relationships and collaborating with multidisciplinary research teams, strong proficiency with REDCap and clinical trial data management systems, and familiarity with FDA regulations, Good Clinical Practice guidelines, and waiver of informed consent or Exception from Informed Consent trial frameworks. This role requires responsiveness in a dynamic acute care research environment with competing operational and regulatory deadlines. Experience in emergency medicine, critical care, or another acute care research setting is highly desirable, particularly experience with cardiac arrest research or pragmatic clinical trials.This is a hybrid role, both with remote work available and on-site presence required. On-site work will primarily be at Harborview Medical Center.**RESPONSIBILITIES:**Multi-Site Oversight (40%)* Serve as the primary liaison between the DEM Research Program and participating study sites, investigators, sponsors, regulatory partners, and collaborating institutions.* Coordinate day-to-day multi-site study operations, including study start-up, site activation, enrollment tracking, ongoing site communication, and study closeout.* Serve as a primary point of contact for site coordinators and investigators regarding participant follow-up and protocol implementation.* Monitor protocol adherence, identify implementation barriers, and collaborate with research leadership to support consistent study procedures and regulatory compliance across sites.* Assist with development of study materials, manuals of procedures, standard operating procedures, and site training resources.* Track study metrics, timelines, adverse events, and reporting requirements; prepare reports for investigators, sponsors, and oversight committees.* Support study financial and operational activities, including invoicing, budgeting coordination, and tracking study supplies and payments.* Ensure compliance with institutional policies, Good Clinical Practice (GCP), HIPAA, FDA regulations, and sponsor requirements.* Maintain oversight of assigned studies, manage competing priorities independently, and support successful trial execution across participating sites.Data Management (15%)* Oversee data collection, entry, quality control, validation, and query resolution using study databases and electronic data capture systems.* Ensure data quality, integrity, and protocol compliance through data cleaning, database management, and audit procedures.* Maintain documentation of data management activities and ensure compliance with study protocols and regulatory requirements.* Develop and implement corrective action plans to address protocol deviations and support data integrity.Regulatory Compliance (15%)* Maintain and update regulatory documentation and study records in compliance with UW IRB, sponsor, HIPAA, and Good Clinical Practice (GCP) requirements.* Prepare and submit IRB applications, renewals, modifications, and continuing reviews; track regulatory approvals and reporting deadlines.* Support audits, monitoring visits, and regulatory reviews by maintaining accurate study documentation and policies and procedures.* Ensure adherence to approved study protocols, data security plans, and institutional compliance requirements. Staff Training (10%)* Develop and deliver onboarding and ongoing protocol training for site coordinators and clinical teams across participating centers.* Oversee onboarding of staff and maintain organized personnel credentials across sites.* Coordinate meetings, trainings, and communications with the DEM research team, multidisciplinary partners, and external collaborators.Study Participant Coordination (10%)* Support participant recruitment, screening, enrollment, consent, and follow-up activities at Harborview and collaborating sites in accordance with study protocols.* Serve as a key resource for participating sites regarding enrollment, follow-up, and protocol adherence and implementation.* Support biospecimen collection, processing, documentation, and transfer in compliance with study procedures.Academic Activities (5%)* Contribute to preparation of study materials, reports, manuscripts, abstracts, posters, and sponsor updates.Other (5%)* Perform 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 2 years of experience coordinating multi-center clinical trials in emergency medicine, critical care, acute care, or a similar clinical setting.* 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:*** Prior clinical research experience in research coordination or project management.* Experience supporting clinical trials and study operations.* Experience with REDCap or other electronic data capture systems.* Strong organizational skills with the ability to manage multiple priorities and timelines independently.* Effective interpersonal and communication skills with demonstrated ability to collaborate in a team environment.* Proficiency with Microsoft Office Suite.* Ability to work occasional evenings and weekends. **DESIRED QUALIFICATIONS**:* Experience coordinating national, multi-site clinical trials.* Experience conducting research in urgent or emergent clinical settings, such as EMS, Emergency Department, or ICU environments.* Experience supporting Exception from Informed Consent (EFIC) studies.* Experience working with multidisciplinary research teams and external collaborators.* Familiarity with statistical software such as STATA or R.* Experience contributing to manuscript preparation, scientific writing, or dissemination of research findings.**Compensation, Benefits and Position Details****Pay Range Minimum:**$65,352.00 annual**Pay Range Maximum:**$120,372.00 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.To request disability accommodation in the application process, contact the Disability Services Office at 206-543-6450 or [e-mail] 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.