Job brief: Clinical Study Monitor

What JoRoute checked · Checked by JoRoute

• Listed on Natera's own job board. JoRoute does not take listings from job ads or recruiters.
• First seen by JoRoute 2026-11-07 (1 day ago); last confirmed on the board 2026-11-08.
• The apply link opens job-boards.greenhouse.io, the address Natera's board gives for this job.
• No other listing with this title and place on this board in the last 90 days.
• No layoff notices (WARN) under this name in the state files JoRoute reads.

What the listing says · Employer's own words, not checked

• Pay: $108,200 to $140,000 a year
• Job type: Not stated
• Where: Remote · US Remote · US
• Posted: 2026-11-06

What the job asks · Employer's own words, not checked

Level: Mid level. The posting asks for 4 years of experience.

Must have

• Manage study documentation, including preparation, review, filing, and archiving in the Trial Master File (TMF).
• Minimum of 4 years of clinical research experience, including at least 2 years monitoring IVD and/or CDx studies.
• Must pass a post-offer criminal background check.
• Certification in clinical research (e.g., ACRP-CP, CCRA, CCRP).
• The pay range is listed and actual compensation packages are based on a wide array of factors unique to each candidate, including but not limited to skill set, years & depth of ex…

Conditions

• Ability to travel up to 40% for site visits, audits, and investigator meetings.
• Physical Demands & Work Environment:
• Duties are performed in a hybrid or office setting requiring computer use, video conferencing, and occasional work during non-standard hours to meet deadlines or coordinate with e…

Main duties

• Serve as the primary point of contact for testing sites, ensuring protocol compliance, subject safety, and data quality align with GCP, FDA, and IVDR require…
• Drive the operational execution of clinical studies, from start-up and site qualification through routine monitoring and close-out.
• Prepare clear, objective monitoring visit reports, tracking site findings, protocol deviations, and CAPAs through to resolution.
• Collaborate across Clinical Operations, Regulatory Affairs, and Quality Assurance to align on study execution and quality expectations.
• Support IRB/EC submission activities and ensure ongoing ethical compliance.

Lines copied from the posting, not rewritten. "Preferred" or "nice to have" items are not listed as must-haves.

How it compares · Compared by JoRoute from listings

• Across Natera's 220 open listings, 31% of those with a posting date were first posted more than 60 days ago. How Natera hires

What nobody outside the employer knows · Not known

• Whether the role is already filled or on hold: employers often leave listings up.
• How many people applied, and who reads the applications.
• Where in the published range an offer would land.

Ask before you apply

1. Is the role fully remote, and from which states can I work?
2. What are the interview steps, and when should I expect to hear back?

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