Clinical Research Coordinator
About The Position
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. The Clinical Research Coordinator will be responsible for various day-to-day tasks related to clinical research, including but not limited to: 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).
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)
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
