On-Site Clinical Research Coordinator: Neuropsychiatry Trials

Seattle Neuropsychiatric Treatment Center PLLC; Washington (District of Columbia); On-site; USD 39,000 - 47,000; Full time

Job summary

Seattle Neuropsychiatric Treatment Center PLLC is seeking a Clinical Research Coordinator for a full-time, on-site role in Seattle, WA, with some flexibility for Bellevue location. The coordinator will handle source documents, consent, scheduling visits, data entry, and lab-related tasks, supporting regulatory work and study visits.

The role requires a Bachelor’s or higher degree in a related field, research experience, and strong organizational and communication skills.

Qualifications

• Bachelor’s or higher degree in related field required.
• Experience in human subjects research and familiarity with implementing research protocols preferred.
• Ability to work independently and prioritize in a dynamic environment.
• Collaborative working across multidisciplinary clinical teams.
• Strong organizational and time management skills for multiple trials.

Responsibilities

• Create source documents for trials and maintain accurate records.
• Manage informed consent process and ensure participant understanding.
• Follow study protocols and schedule research visits.
• Perform data entry and maintain data integrity.
• Coordinate with Sponsor and CROs and address queries.
• Support regulatory activities and study visits (lab shipments, room prep).

Skills

Organizational skills

Communication skills

Independent work

Team collaboration

Problem solving

Attention to detail

Education

Bachelor’s or higher degree in related field

Certified Clinical Research Professional or CCRP/CCRC

Tools

Excel

Word

SharePoint

EMR systems

CTMS

Job description

Seattle Neuropsychiatric Treatment Center PLLC is seeking a Clinical Research Coordinator for a full-time, on-site role in Seattle, WA, with some flexibility for Bellevue location. The coordinator will handle source documents, consent, scheduling visits, data entry, and lab-related tasks, supporting regulatory work and study visits.

The role requires a Bachelor’s or higher degree in a related field, research experience, and strong organizational and communication skills.