Research Coordinator 3 (E S UAW Research)

University of Washington•Seattle, WA

6d•$78,600 - $130,668•Onsite

About The Position

The Division of Pulmonary Critical Care and Sleep Medicine has an outstanding opportunity for a Research Coordinator 3 to join their team. Reporting to the Research Manager, the Research Coordinator will take a lead role in conducting and managing a clinical research program undertaking studies that focus on the adult cystic fibrosis patient population.

Requirements

Bachelor's degree in a health sciences related field with 4 years of relevant experience.
Clinical research operations experience including project management and long range planning.
Excellent verbal, written and interpersonal communication skills.
Demonstrated problem-solving skills, strong detail orientation and ability to adeptly manage multiple priorities and timelines.
Ability to work with various individual working styles and organizational systems is necessary.

Nice To Haves

Familiarity with UW research policies and guidelines including IRB development, budget development and budget management.
Fluency in Spanish, with the ability to conduct study visits and patient interviews in Spanish, is preferred.

Responsibilities

Collaborating on implementation and ongoing management of CF clinical trials being conducted at the UW and collaborating sites.
Implementing assigned aspects of data collection and ensuring UW site subject compliance and adherence with protocol requirements.
Tracking milestone achievements for the site while responding to data queries and assuring data entry accuracy.
Identifying, screening, recruiting, and consenting subjects for UW site participation.
Administering a wide variety of clinical survey instruments and conducting study visits with patients.
Responsible for IRB submissions using both UW and private IRB systems and direct response to Human Subjects Office and Office of Sponsored Programs.
Assisting with developing study manuals and case report forms in compliance with extramural sponsor and UW compliance office guidelines.
Ensuring accurate tracking and timely payment of study subject stipends and/or travel reimbursements.
Investigating and documenting study costs for grant or contract proposals and post-award expenditure management.
Utilizing clinical trial management systems to review clinical charges.