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Natera
Clinical Study Monitor
Remote · US Remote · Full time · Mid level
$108k–$140k / year
About the role
Oversee execution and monitoring of clinical studies for in vitro diagnostic devices. Ensure compliance with protocols, SOPs, and regulatory requirements while prioritizing data quality and subject safety.
What you’ll do
• Serve as primary contact for testing sites. • Execute monitoring activities per study plan. • Drive clinical study operations from start-up to close-out. • Prepare monitoring visit reports and track findings. • Support audit readiness and regulatory inspections.
What you’ll bring
• BA/BS in life sciences or related field. • 4+ years clinical research experience. • Knowledge of GCP, FDA, IVDR regulations. • Ability to travel up to 40%. • Must pass criminal background check.
Life at Natera
Offers comprehensive medical, dental, vision, life and disability plans. Provides fertility care benefits, pregnancy and baby bonding leave, 401k, commuter benefits, and employee referral program.
About Natera
Natera is a global leader in cell-free DNA testing focused on oncology, women’s health, and organ health, aiming to make personalized genetic testing standard care.