Clinical Research Associate

What you’d do

Ensure regulatory compliance for clinical trials by working with clinical teams, IRBs, sponsors, and federal agencies. The role is full time and involves monitoring data integrity and protocol adherence without patient care duties. Found on the employer's careers page on Oct 26, 2026. Apply through the link.

You’ll need

• Attention to detail
• Knowledge of clinical research protocols
• Effective communication skills
• Ability to recognize compliance and data integrity issues