Clinical Research Associate Jobs in Washington

Inland Northwest Research (INWR) is a clinical research center specializing in Parkinson's disease, Huntington's disease, and other neurological movement disorders. Working closely with Selkirk Neurology, we conduct clinical trials investigating promising new treatments for patients with neurological conditions.

We are seeking a Clinical Research Coordinator (CRC-I or CRC-II) to join our growing research team. We will consider candidates at different experience levels, from those developing their clinical research careers to experienced coordinators capable of independently managing complex clinical trials.

This is a hands-on, patient-facing position requiring excellent organizational skills, strong attention to detail, and a commitment to conducting high-quality clinical research.

Key Responsibilities

• Coordinate clinical trial activities, including participant screening, informed consent, enrollment, study visits, and follow-up.
• Schedule and conduct research visits, coordinating with investigators, nursing staff, participants, and caregivers.
• Maintain accurate and timely source documentation, electronic data capture (EDC) records, and study logs.
• Monitor protocol compliance, identify potential deviations, and escalate participant safety or data quality concerns.
• Prepare for monitoring visits, respond to data queries, and communicate with sponsors and clinical research organizations (CROs).
• Support regulatory documentation, study startup, and inspection readiness.
• Perform or coordinate study procedures, including vital signs, ECGs, clinical assessments, and laboratory collections, as appropriately trained and authorized.
• Work collaboratively with other coordinators while maintaining accountability for assigned studies and responsibilities.

Experience Levels

Clinical Research Coordinator I (CRC-I): $28–$33/hour

An early-career coordinator who can conduct routine study activities with appropriate guidance and progressively assume responsibility for assigned trials. Prior clinical research experience is preferred, although candidates with strong patient-facing healthcare or related research experience may be considered.

Clinical Research Coordinator II (CRC-II): $34–$40/hour

An experienced coordinator capable of independently managing clinical trials, including complex study visits, sponsor and monitor communication, source documentation, regulatory compliance, and data quality. Requires at least 18 months of direct clinical trial experience and demonstrated independent study coordination. Three or more years of clinical research experience is preferred.

Qualifications

• Excellent attention to detail, organizational skills, and ability to manage competing priorities.
• Strong communication skills and comfort working directly with patients and caregivers.
• Familiarity with clinical trial documentation, electronic data systems, and Good Clinical Practice (GCP).
• Ability to independently manage responsibilities, meet deadlines, and identify issues requiring escalation.
• Bachelor's degree in a health, science, or related discipline preferred; relevant experience considered.
• CITI Human Subjects Protection and GCP training required before performing delegated study activities.
• Clinical research certification (CCRC or CCRP), phlebotomy certification, or relevant clinical licensure preferred.
• Experience in neurology, movement disorders, or pharmaceutical-sponsored clinical trials is particularly desirable.

Schedule and Location

This is a full-time, in-person position in Spokane, Washington, working five days per week. Occasional early morning, evening, or weekend availability may be required to accommodate clinical study visits.

This is not a remote or hybrid position.

Compensation and Benefits

• CRC-I: $28–$33 per hour.
• CRC-II: $34–$40 per hour.
• Medical, dental, and vision insurance.
• Paid leave and other benefits in accordance with company policies.
• Training and opportunities for professional development in clinical research.

Employment Eligibility

Applicants must be legally authorized to work in the United States. Inland Northwest Research is unable to provide employment-based visa sponsorship, either now or in the future.

We welcome candidates interested in building a long-term career in clinical research, with opportunities to develop expertise in neurological clinical trials and participate in important research advancing treatment options for patients with movement disorders.

Pay: $28.00 - $40.00 per hour

Expected hours: 40.0 per week

Benefits:

• 401(k)
• 401(k) matching
• Health insurance
• Life insurance
• Paid time off
• Retirement plan
• Vision insurance

Application Question(s):

• Will you now or in the future require employer sponsorship for U.S. employment visa status?
• This position requires working on-site in Spokane, Washington, five days per week. Are you able to meet this requirement?
• Have you independently managed a clinical trial as the primary study coordinator, including participant visits, documentation, and sponsor or monitor communication?
• Briefly describe your direct experience with informed consent, participant visits, source documentation, EDC data entry, and sponsor monitoring. Which of these responsibilities have you personally performed?
• Are you comfortable with the advertised compensation ranges of $28–$33/hour for CRC-I or $34–$40/hour for CRC-II, depending on qualifications?
• Answer in your resume or cover letter: How much direct clinical trial experience do you have?

None

Less than 1 year

1–2 years

2–3 years

More than 3 years

Work Location: In person