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Clinical Research Nurse Coordinator

Full Time - Redmond, WA

Eastside Research Associates is a fast-growing clinical research company that is seeking a highly motivated Clinical Research Nurse Coordinator to assist with a variety of ongoing clinical trials. This includes day to day operations, nursing care and assessment for patients enrolled in research studies, patient care, coordination with Principal Investigators for individual studies, maintaining complete and comprehensive records for the research operation and organizational tasks. Someone who has worked in a high paced, fast moving environment will work well at Eastside Research Associates. The schedule for this position will be Monday- Friday, 8:00AM-5:00PM with occasional evening or weekend hours needed.

Essential Responsibilities

  • Provide coordination and oversight for the execution of clinical trials

  • Review study candidates’ medical records for study eligibility

  • Consent patients for clinical research studies

  • Monitor and maintain case report forms, charts and documentation.

  • Perform vital signs, venipuncture/phlebotomy, peripheral IV insertion and infusions, nasal swabs and medication dispensing and tracking as needed for studies

  • Ensure strict compliance with established research protocols and standards along with all applicable laws, regulations, policies, and procedural requirements

  • Serve as a liaison between clinical teams, patients, and sponsors

  • Provide input regarding IRB correspondence and regulatory documentation. Submit documentation as required

  • Follow established SOPs, GCP and other applicable regulatory requirements in the execution of all research activities.

  • Other duties as assigned


  • Current Washington State RN licensure is required

  • Minimum 2 years of nursing experience

  • Ability to work independently with minimal supervision

  • Ability to effectively collaborate with other team members

Desired Skills & Qualifications

  • Excellent written and verbal communication skills

  • Experience with Microsoft Office

  • High attention to detail

  • Strong organizational and time management skills

  • Outstanding patient care skills

  • Knowledge of clinical research operations, including Good Clinical Practice guidelines is preferred

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