Analyst II - Clinical Trials Operations

What you’d do

Independently manage a portfolio of clinical research studies through start-up and activation, building study records in CTMS/EMR systems, performing quality reviews, and reporting progress to leadership. Full time; also mentors junior staff. Found on the employer's careers page on Oct 7, 2026. Apply through the link.

You’ll need

• 2 years clinical research operations experience
• CTMS/EMR builds or study start-up competency
• Independently manage study start-up activities
• Quality review and status reporting experience