Position Summary:
The Clinical Research Coordinator I is responsible for a variety of activities in support of clinical research studies. The Clinical Research Coordinator I is responsible for the implementation of clinical studies at all levels, including but not limited to: IRB applications and related forms, data collection forms, patient screening and enrollment, data analysis, sponsor/IRB communications, verification of investigative procedures to accomplish research goals, and preparation of reports. The Clinical Research Coordinator I develops and implements research project procedures that meet research objectives and ensure compliance with all aspects of Institution, Federal Drug Administration (FDA) and sponsor regulations pertaining to clinical research in human subjects (e.g. investigator financial disclosure requirements of the FDA).
Work situations are varied and require strong organization, prioritization, data analysis, verbal and written communication skills, use of discretion, good judgment, problem solving, decision-making and leadership. This position requires interaction with a wide variety of internal and external groups to include nursing staff, management, physicians, patients, outside organizations, research groups and service groups such as laboratories, pharmacy and radiology.

Minimum Requirements:
One (1) year of research experience within a healthcare setting or four (4) years’ experience in research industry in a research position
Prior experience as a research assistant or coordinator strongly preferred

Education/Licenses/Certifications:
Bachelors’ degree preferably in science, healthcare or other related fields required. Equivalent combination of education and experience may be substituted for the degree
Valid Washington State driver's license
Depending on assigned area one of the following is required:
Medical Assistant – Phlebotomy (if duties include venous blood draws)
Medical Assistant – Registered (if duties do not include venous blood draws)