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Clinical Research Coordinator

Full Time - Redmond, WA

Eastside Research Associates is a fast-growing medical research company that is seeking an experienced, professional Clinical Research Coordinator to execute clinical research studies according to ICH/GCP guidelines and FDA regulations. We are looking for someone who can take initiative and coordinate multiple studies at one time. Someone who has worked in a high paced, fast moving environment will work well at Eastside Research Associates. Previous experience in a private researching setting is a must.

Responsibilities

  • Review study candidates’ medical records for study eligibility

  • Consent patients for clinical research studies

  • Maintain case report forms, charts and documentation.

  • Take EKGs and vital signs

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

  • Data collection and entry

  • Manage investigational devices and and drug inventory

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

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

Requirements

  • Clinical skills; nursing, MA or equivalent

  • Minimum 2 to 3 years of clinical research coordinator experience in a private research setting- no academic research experience

  • Excellent communication and organizational skills

  • Detail-oriented

  • Strong organizational and time management skills

  • Familiarity with the Code of Federal Regulations as they pertain to human subject protection

  • Strong computer skills'

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