The primary responsibility of the research coordinator is to manage all aspects of conducting clinical trials. The research coordinator is required to have an in-depth knowledge of protocol requirements and good clinical practices as set forth by federal regulations. As the primary resource for the protocols, the research coordinator will act as liaison between the investigators, primary care providers, the institutional review board (IRB), and the sponsor. Along with the investigator, the research coordinator will screen, enroll and follow study subjects, ensuring protocol compliance and close monitoring while the subjects are on study. In addition, the coordinator is responsible for all data and source documentation, adverse experience reporting, and maintenance of complete regulatory files. Additionally the research coordinator will assist the project manager in developing a diverse research portfolio, educational outreach to regional support groups and area providers.

Qualifications for CRC

• Minimum baccalaureate (BA/BS) in a health-related field and at least two (2) years of clinical research-related experience required.
• Sound knowledge of the clinical trial process, including but not limited to recruitment, screening, enrollment, and follow-up of eligible subjects according to protocol requirements (e.g., subject follow-up, case report form completion, and reporting of adverse drug experiences).
• Maintenance of accurate and complete documentation, including not but limited to regulatory documents, signed informed consent forms, relevant IRB approvals, source documentation, drug dispensing logs, subject logs, and study-related communications.
• Organizational management of all aspects of the trial, including but not limited to timeliness in completing case report forms (CRFs), data entry, reporting adverse drug effects (ADEs), managing caseload and managing study files.
• Communication of all protocol-related issues/problems to the appropriate management staff, including but not limited to questions regarding the conduct of the clinical trial, concerns regarding possible AEs or subject compliance.
• Professional conduct in the presence of subjects, research staff, sponsors, monitors, etc.

*Research experience required*

About Us: Inland Northwest Research is a private biomedical research company in Spokane, WA specializing in neurodegenerative clinical trials. We focus on movement disorders such as Parkinson's Disease, Huntington's Disease, Essential Tremor and Multiple System Atrophy. We are passionate about furthering science for the betterment of our patients and their families by running many of the top clinical trials in the world. We are looking for someone to join our team who is motivated and driven by the desire to do the same.

Job Type: Full-time

Pay: $25.00 - $35.00 per hour

Benefits:

• 401(k)
• 401(k) matching
• Dental insurance
• Flexible schedule
• Health insurance
• Paid time off
• Parental leave
• Vision insurance

Schedule:

• 8 hour shift
• Monday to Friday

Work Location: One location

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