Start Date
Immediate
Expiry Date
19 Sep, 25
Salary
34.99
Posted On
20 Jun, 25
Experience
2 year(s) or above
Remote Job
Yes
Telecommute
Yes
Sponsor Visa
No
Skills
Access, Veterans Affairs, Documentation, Compliance Regulations, Hcp, Qualtrics, Excel, Communication Skills, Microsoft Applications, Participation, Outlook, Drug Testing
Industry
Hospital/Health Care
Title: Clinical Research Coordinator
Job Class: Hourly/Non-Exempt; $28.92-34.99/hr
PI: Dr. Laura Feemster
At the Seattle Institute for Biomedical and Clinical Research (SIBCR), scientists seek new ways to improve the health and well-being of Veterans through research and education conducted at the VA Puget Sound Health Care System (VAPSHCS) and Mann-Grandstaff VA Medical Center. You will also enjoy outstanding benefits, professional growth opportunities, and the chance to be a part of an important mission.
SIBCR’s research spans a broad range of areas such as mental health; neuroscience; diabetes, endocrinology and nutrition; prosthetics; oncology; age-related diseases; and, pulmonary diseases. We are seeking a Clinical Research Coordinator for Dr. Laura Feemster research programs.
SUMMARY:
The Clinical Research Coordinator will work as a key team member on the Functional improvement in OSA and COPD with a Telehealth LifeStyle and Exercise Intervention (FOCuSEd) Study sponsored by the Patient-Centered Outcomes Research Institute (PCORI). This position is a pulmonary study based at the Mann Grandstaff VA Medical Center in Spokane, WA and will require an individual who understands the principles of scientific investigation and clinical trials and is capable of in-depth understanding of the study protocol. The candidate must possess strong scientific, organizational, and interpersonal skills. The position is full-time, Monday through Friday. Salary will be based according to the applicant’s research experience and includes benefits.
PREFERRED KNOWLEDGE AND EXPERIENCE WITH:
Required Knowledge and Experience:
Leading recruitment, screening, enrollment, consent, and follow-up of clinical trial participants according to study protocol, including:
Required Knowledge and Experience: