Clinical Study Monitor

📋 Description

• Serve as the primary point of contact for testing sites, ensuring protocol compliance, subject
• Execute monitoring activities based on the study-specific plan, including source data verification
• Drive the operational execution of clinical studies, from start-up and site qualification through
• Prepare clear, objective monitoring visit reports, tracking site findings, protocol deviations, and
• Take ownership of developing study-related documents, relying on strong judgment to move work
• Collaborate across Clinical Operations, Regulatory Affairs, and Quality Assurance to align on study

🎯 Requirements

• BA/BS degree in life sciences, nursing, or a related field (advanced degree such as MS or MPH is a
• Minimum of 4 years of clinical research experience, including at least 2 years monitoring IVD
• Strong knowledge of GCP, ISO 20916, IVDR, and/or FDA regulations (21 CFR Part 812) relevant to
• Working knowledge of diagnostic laboratory operations.
• Ability to travel up to 40% for site visits, audits, and investigator meetings.
• Must pass a post-offer criminal background check.

🎁 Benefits

• Competitive Benefits - Employee benefits include comprehensive medical, dental, vision, life and
• Additionally, Natera employees and their immediate families receive free testing in addition to
• Other benefits include pregnancy and baby bonding leave, 401k benefits, commuter benefits and much
• We also offer a generous employee referral program!