# Clinical Study Monitor at Natera

- Company: Natera
- What the company does: Dedicated to oncology, women’s health, and organ health. Natera’s cell-free DNA tests help protect health and inform more personalized decisions about care. Backed by Lightspeed and Sequoia.
- Company website: https://natera.com/
- Type: Startups
- Level: Mid level
- Location: US Remote
- Work setup: Remote
- Posted: 2026-11-06
- Apply by: 2026-12-21
- Apply: https://job-boards.greenhouse.io/natera/jobs/6242431004?utm_source=1752vc&utm_medium=careers
- Page: https://www.1752.vc/careers/jobs/natera-clinical-study-monitor/

## About the role

Serve as the primary point of contact for testing sites, ensuring protocol compliance, subject safety, and data quality align with GCP, FDA, and IVDR requirements. Execute monitoring activities based on the study-specific plan, including source data verification (SDV), essential document review, specimen tracking, and resolving sample handling issues. Found on 1752vc Careers, the job board for startup and VC roles.

## What they're looking for

- BA/BS degree in life sciences, nursing, or a related field (advanced degree such as MS or MPH is a plus)
- Minimum of 4 years of clinical research experience, including at least 2 years monitoring IVD and/or CDx studies
- Strong knowledge of GCP, ISO 20916, IVDR, and/or FDA regulations (21 CFR Part 812) relevant to diagnostic studies
- 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

Tags: Clinical Trials

Source: 1752vc Careers, https://www.1752.vc/careers/jobs/natera-clinical-study-monitor/