Clinical Research Coordinator

About This Role

This Clinical Research Coordinator role is responsible for the day-to-day coordination of clinical trials for neuropsychiatric disorders, including managing study documentation, patient visits, and data entry. The goal is to contribute to advancing innovative treatments at SeattleNTC.

Responsibilities

• Create source documents
• Manage the informed consent process
• Follow research protocols
• Schedule and conduct research visits
• Perform data entry
• Handle laboratory processes
• Communicate with the Sponsor and CROs
• Address queries
• Support study regulatory work and research visits (e.g., shipping labs, study room preparation)

Requirements

• Bachelor’s or higher degree in related field
• Experience in human subjects research and familiarity with implementing research protocols
• Ability to work independently and prioritize work in a dynamic environment
• Ability to work across multidisciplinary teams
• Resourceful and able to solve problems, yet seek guidance when needed
• Ability to learn quickly
• Excellent organizational skills; ability to manage time with multiple tasks and working on multiple trials
• Comfortable working in clinic setting and interacting with patients
• Strong attention to detail
• Exceptional interpersonal skills both in-person and on telephone calls
• Strong written and verbal communication skills
• Experience with Excel, Word, SharePoint, and other computer productivity software

Qualifications

• Bachelor’s or higher degree in related field
• Experience in human subjects research and familiarity with implementing research protocols

Nice to Have

• Knowledge of FDA regulations, GCP guidelines, and other applicable regulations
• Ability to work according to Standard Operating Procedures (SOPs)
• Certified Clinical Research Professional or Certified Clinical Research Coordinator accreditation
• Experience working with electronic medical records (EMR) and a clinical trial management system (CTMS)
• Experience and certification in rating scales (eg, MINI, C-SSRS, SDS, CAPS-5)
• Previous experience in interventional clinical trials for at least 1 year

Skills

* Required skills