Clinical Research Associate II, Phase I

This is a fully remote position, open to applicants in Kansas, +1 more state.

📋 Description

• Oversee all components of study site monitoring, including routine checks and the closing of clinical sites.

• Perform pre-study assessments and initiation visits.

• Ensure compliance with informed consent procedures and protocol guidelines.

• Review data for any missing or implausible entries.

• Complete reporting for Serious Adverse Events (SAEs).

• Support the training of new staff members.

⛳️ Requirements

• A university or college degree, or certification in a relevant allied health field from a recognized institution (e.g., nursing license).

• A minimum of 1 year of experience in Clinical Monitoring.

• Experience in Phase I clinical trials.

• Willingness to travel overnight 40-50% of the time.

🏝️ Benefits

• Health insurance coverage.

• Flexible working arrangements.

• Opportunities for professional development.