Clinical Research Coordinator

Seattle Neuropsychiatric Treatment Center PLLC • Seattle, WA

21d • $28 - $34 • Onsite

About The Position

Seattle Neuropsychiatric Treatment Center (SeattleNTC) specializes in innovative treatments for depression and difficult-to-treat neuropsychiatric disorders, including Transcranial Magnetic Stimulation (TMS), Electroconvulsive Therapy (ECT), esketamine, and more. With locations in Seattle, Bellevue, Tacoma, Bellingham, and Poulsbo, we provide comprehensive care options for our patients. Our clinical trials program, housed in our Seattle and Bellevue locations, focuses on studying interventions for psychiatric disorders. We are currently participating in trials on VNS for bipolar depression, psilocybin for depression and anxiety, and a new version of TMS, among others. Our research team consists of two managers, eight coordinators (CRC, recruitment, and regulatory), and several PI/sub-Is. This is an exciting opportunity to contribute to the advancement of innovative treatments in the field of neuropsychiatry. This is a full-time on-site role for a Clinical Research Coordinator at our Seattle, WA location; we value some flexibility to also work at our Bellevue location.

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
• Collaborative and skilled working across multidisciplinary teams including clinical 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; fast at learning computer skills

Nice To Haves

• 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

Responsibilities

• Creating source documents
• Managing the informed consent process
• Following protocols
• Scheduling and conducting research visits
• Data entry
• Laboratory processes
• Communicating with the Sponsor and CROs
• Addressing queries
• Supporting study regulatory work and research visits (e.g., shipping labs, the study rooms preparation).

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level