As a Senior Contract Analyst, you will manage agreements, ensure compliance, and support project teams in contract interpretation and execution.

The Study Start-Up Lead will manage country-level study start-up activities, handle IRB submissions, ensure timely site selection, and improve operational processes.

As a Clinical Research Associate, you'll conduct site visits for clinical trials, ensuring compliance and data integrity, and collaborating with investigators.

Coordinate study activities, monitor trials, submit documentation, and assist in training other CRAs while ensuring compliance with GCP guidelines.

The Site Partner II coordinates activities for timely site activation in clinical trials, serving as the main liaison for site issues, ensuring compliance with regulatory standards and maintaining documentation accuracy.