Medical Monitor

What you’d do

Provides day-to-day medical oversight for clinical trials, including safety signal evaluation, eligibility assessments, dose modifications, and risk mitigation. Works with clinical operations, pharmacovigilance, data management, and regulatory teams. Full time, remote. Found on the employer's careers page on Oct 21, 2026. Apply through the link.

You’ll need

• MD or equivalent medical degree
• 3–7 years in clinical trial execution or medical monitoring
• Knowledge of GCP and safety reporting requirements
• Experience reviewing AEs/SAEs and safety oversight