Clinical Research Coordinator I - Trials & Compliance

ERA Health Research; Redmond (WA); On-site; USD 41,000 - 45,000; Full time

Benefits offered by this job

Medical Insurance

401k Plan

PTO starting 10 days

Job summary

ERA Health Research in Redmond, WA seeks a full-time Clinical Research Coordinator I to join our Clinical Operations team. The role coordinates all aspects of clinical trials, ensuring ethical, regulatory, and scientific standards and maintaining participant safety and data integrity.

Responsibilities include preparing study materials, coordinating visits, handling informed consent, managing documentation, and supporting monitoring activities.

Qualifications

• 1–2 years of clinical research experience.
• Basic understanding of scientific terminology.
• Must obtain WA MA-R and MA-P credentials within a defined timeframe.
• Proficient with MS Office.

Responsibilities

• Identify objectives and outcome measures for trials.
• Coordinate protocol adherence and protocol amendments per GCP.
• Schedule and prepare site initiation visits and regulatory documents.
• Ensure SOPs align with study requirements and maintain data integrity.
• Identify trial supplies and manage inventory to support the study.
• Develop trial management tools and subject calendars for compliance.
• Complete pre-screening, screening and enrollment logs accurately.
• Coordinate regulatory, recruitment and clinical staff visits.
• Obtain informed consent and randomize subjects per protocol.
• Support investigational product handling and shipping.
• Collect, ship and store specimens per requirements.
• Educate and communicate with subjects throughout the trial.
• Document monitoring visits and follow-up actions and address queries.

Skills

Clinical Research

Regulatory Compliance

GCP Knowledge

Data Integrity

Communication Skills

Team Collaboration

MS Office

Education

Bachelor's in Life Sciences

Tools

MS Office

Job description

ERA Health Research in Redmond, WA seeks a full-time Clinical Research Coordinator I to join our Clinical Operations team. The role coordinates all aspects of clinical trials, ensuring ethical, regulatory, and scientific standards and maintaining participant safety and data integrity.

Responsibilities include preparing study materials, coordinating visits, handling informed consent, managing documentation, and supporting monitoring activities.