Entry-Level Clinical Research Coordinator Phase IV Trials

American Oncology Management Company; Olympia (WA); On-site; USD 33,000 - 47,000; Full time

Job summary

Vista Oncology is seeking a Clinical Research Coordinator I (non-RN) to oversee the implementation and ongoing management of its clinical research studies. This role involves coordinating entry-level protocol designs and ensuring adherence to regulatory requirements across multiple trials.

The position requires basic knowledge of clinical research, regulatory processes, and data handling, with a focus on accumulation of 5 trials open to accrual annually and patient flow of 2–10 per year.

Qualifications

• High school education required.
• Some college is preferred.
• Prior research or related medical science experience.

Responsibilities

• Coordinate care for patients on clinical research protocols in accordance with GCP/ICH/FDA guidelines and requirements.
• Prepare and monitor regulatory documents and ensure data accuracy.
• Assist with budgeting and study billing compliance.
• Support monitoring visits and respond to sponsor/IRB requests.

Skills

Communication Skills

Interpersonal Effectiveness

Analysis & Critical Thinking

Self-Management

Attention to Detail

Education

High school education

Some college

Tools

MS Office

EMR

EDC

CTMS

Job description

Vista Oncology is seeking a Clinical Research Coordinator I (non-RN) to oversee the implementation and ongoing management of its clinical research studies. This role involves coordinating entry-level protocol designs and ensuring adherence to regulatory requirements across multiple trials.

The position requires basic knowledge of clinical research, regulatory processes, and data handling, with a focus on accumulation of 5 trials open to accrual annually and patient flow of 2–10 per year.