Research Coordinator ; Temporary

## Research Coordinator 3 (Temporary)
Apply remote type:
No Teleworklocations:
Seattle, WAtime type:
Full time posted on:
Posted Todayjob requisition :
REQ
- ** Job Description
**** The Department of Medicine, Division of Metabolism, Endocrinology and Nutrition, has an outstanding opportunity for a temporary Research Coordinator 3 to join their team.
**** About this Opportunity
** Reporting to the Professor, the Research Coordinator 3 serves as a senior-level coordinator and subject-matter expert overseeing the implementation and execution of multiple complex clinical research studies in the lipid/cardiometabolic space under the PI Dr Subramanian. The ideal candidate will have a strong background in cardiometabolic research.
** Key Responsibilities
** Research protocol management (60%):
* Independently provide operational oversight initiation and implementation of multiple concurrent clinical research protocols for PI.
* Align clinical activities with study protocols, including time-sensitive visit scheduling and sample shipment preparation.
* Ensure accuracy and integrity of research data through rigorous verification, audit preparation, and compliance monitoring.
* Take a lead role in preparing, submitting and maintaining Institutional Review Board (IRB) documentation, including new applications, amendments, and continuing reviews.

Participant management (30%):
* Lead strategic recruitment initiatives ensuring accurate eligibility screening in accordance with IRB and protocol-specific criteria.
* Recruitment, screening, and enrolling study participants who meet research criteria.

Administration (10%):
* Serve as a key liaison to study sponsors and monitors, ensuring alignment with contractual timelines and expectations.
* Partner with fiscal staff to manage reimbursement workflows for participant expenses and study-related operational costs, ensuring timely and accurate financial stewardship.
* Collaborate with PI on other project management duties as assigned and proactively identify additional areas for support.
** 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
** Applicants who do not meet these qualifications WILL NOT be forwarded to the Hiring Manager.
* Bachelor’s degree in science or health related field and four years of relevant experience in clinical research.
** Additional Qualifications
*** Experience in clinical research related to lipids and/or diabetes.
* Prior experience in an academic research environment.
* Prior clinical and laboratory research experience.
* Experience with project coordination.
* Experience with data collection for human health research.
* Knowledge of human subjects research, including study implementation, data analysis, regulatory compliance, and IRB processes.
* Demonstrated ability to work independently with flexibility and manage multiple clinical research protocols simultaneously.
* Strong written and verbal communication, organizational, and time-management skills.
* Detail-oriented with a high degree of accuracy in all aspects of work.
* Team player with a positive outlook and the highest degree of professionalism.
** Preferred Qualifications
*** Familiarity with FDA regulations.
* Certification in Good Clinical Practices.
* Appropriate clinical research training including CITI, HIPAA.
* Strong proficiency with Epic electronic medical record system, knowledge of medical terminology.
** Compensation, Benefits and Position Details
**** Pay Range…