RN Clinical Research Coordinator — Trials & Compliance

ERA Health Research; Redmond (WA); On-site; USD 128,943,000 - 143,270,000; Full time

Benefits offered by this job

Medical, dental, and vision insurance

401k Retirement Savings Plan

Paid time off (PTO)

Floating holidays

Job summary

ERA Health Research in Redmond, WA seeks a Clinical Research Nurse Coordinator I to coordinate all aspects of clinical trials, ensuring ethical, regulatory, and scientific standards with participant safety and data integrity. Active, unrestricted RN licensure in Washington is mandatory.

Responsibilities include trial setup, consent, data entry into EDC, specimen handling, and collaboration with cross-functional teams.

Qualifications

• Active, unrestricted Washington RN license required upon hire.
• At least 1 year clinical and/or clinical research experience.
• Current CPR or Basic Life Support (BLS) certification, or ability to obtain within first 90 days.
• Venipuncture and IV start skills or ability to learn within first 30 days.
• Meticulous attention to detail with ability to follow complex instructions.
• Strong organizational and problem-solving skills.
• Teamplayer with good written and verbal communication.
• Proficient with MS Office.
• ERA does not provide employment visa sponsorship; must be authorized to work in the United States without sponsorship.
• Relocation assistance is not available.

Responsibilities

• Identify objectives, endpoints and outcome measures for a given clinical trial.
• Implement protocol and amendments per GCP, verify IRB/IEC approved documents.
• Schedule, coordinate, and prepare documents, equipment, facilities for site initiation visits.
• Complete training and interpret study implementation plan for priority items.
• Ensure SOPs align with study requirements.
• Identify required study supplies and reconcile inventory.
• Develop trial management tools to enhance subject compliance.
• Complete pre-screening, screening and enrolment logs and forms.
• Coordinate with regulatory, recruitment, and clinical staff to schedule patient visits.
• Complete informed consent and randomization per protocol.
• Support and manage investigational product labeling, preparation and dispensing.
• Perform nursing assessments and protocol-related procedures.
• Administer investigational products and monitor patient responses.
• Assess, document and report Adverse Events and SAEs.
• Manage patient education and visit schedule compliance.
• Document and report any unanticipated problems per GCP.
• Schedule and prepare monitoring visits and follow-up activities.
• Collect, ship, and store specimens per requirements.
• Maintain regulatory documents and study binders.
• Train new team members on clinical research skills.
• Travel to other company sites as needed.

Skills

Clinical research

RN licensure

CPR/BLS

Venipuncture

MS Office

Communication

Organizational skills

Team player

Education

CPR/BLS certification

Tools

EDC systems

Job description

ERA Health Research in Redmond, WA seeks a Clinical Research Nurse Coordinator I to coordinate all aspects of clinical trials, ensuring ethical, regulatory, and scientific standards with participant safety and data integrity. Active, unrestricted RN licensure in Washington is mandatory.

Responsibilities include trial setup, consent, data entry into EDC, specimen handling, and collaboration with cross-functional teams.