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Clinical Trial Risk Based Monitoring Jobs in Austin, TX

Neuralink

Clinical Research Associate

Austin, TX · On-site

From navigating regulatory pathways, designing trial protocols and documentation, and executing ... Familiarity with risk-based monitoring approaches * Exposure to early feasibility or first-in-human ...

IQVIA

Clinical Trial Psych Rater

Austin, TX · Remote

$62K - $156K/yr

Clinical Trial Psych Rater - US Spanish Speaking Location: Remote/Virtual Hours: Estimated 10-16 ... The actual base pay offered may vary based on a number of factors including job-related ...

YO AI Labs

Clinicia Expert - Remote

Austin, TX · Remote

$150 - $200/hr

Review benefit-risk assessments and identify clinically inconsistent, inaccurate, or implausible ... monitor, safety physician, or clinical development physician. * Experience reviewing clinical trial ...

YO AI Labs

Oncology Expert - Remote

Austin, TX · Remote

$150 - $200/hr

Review benefit-risk assessments and identify clinically inconsistent, inaccurate, or implausible ... monitor, safety physician, or clinical development physician. * Experience reviewing clinical trial ...

YO AI Labs

Hematology Expert - Remote

Austin, TX · Remote

$150 - $200/hr

Review benefit-risk assessments and identify clinically inconsistent, inaccurate, or implausible ... monitor, safety physician, or clinical development physician. * Experience reviewing clinical trial ...

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Clinical Trial Risk Based Monitoring information

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How much do clinical trial risk based monitoring jobs pay per hour?

As of Aug 23, 2026, the average hourly pay for clinical trial risk based monitoring in Austin, TX is $39.63, according to ZipRecruiter salary data. Most workers in this role earn between $31.92 and $43.61 per hour, depending on experience, location, and employer.

What is clinical trial risk based monitoring?

Clinical Trial Risk Based Monitoring (RBM) is a strategy used in clinical research to prioritize and focus monitoring activities on the most critical risks to patient safety and data integrity. Instead of monitoring every data point equally, RBM uses data analytics and risk assessment tools to identify which sites, processes, or data require more attention. This approach increases efficiency, reduces costs, and helps ensure that potential issues are detected and addressed promptly. RBM is supported by regulatory agencies and is increasingly adopted in both large and small clinical trials.

How does a clinical trial risk based monitoring professional typically collaborate with cross-functional teams during a study?

In a Clinical Trial Risk Based Monitoring role, you will regularly work with clinical research associates, data managers, statisticians, and regulatory teams to identify and address potential risks throughout a study. Collaboration often involves participating in meetings to review data trends, sharing insights about site performance, and helping to develop mitigation strategies. Effective communication is crucial, as you will be responsible for ensuring that all stakeholders are informed of key risks and recommended actions. This collaborative environment helps drive patient safety, data integrity, and overall trial success.

What are the key skills and qualifications needed to thrive in clinical trial risk based monitoring, and why are they important?

To thrive in Clinical Trial Risk Based Monitoring, you need expertise in clinical research, regulatory compliance, and data analysis, usually supported by a degree in life sciences or related fields. Familiarity with risk assessment tools, EDC (Electronic Data Capture) systems, and GCP (Good Clinical Practice) certification is typically required. Strong attention to detail, critical thinking, and effective communication help professionals proactively identify and address potential risks in trials. These skills are crucial for maintaining data integrity, ensuring patient safety, and optimizing the efficiency and quality of clinical studies.

What is the difference between Clinical Trial Risk Based Monitoring vs Clinical Trial Data Manager?

AspectClinical Trial Risk Based MonitoringClinical Trial Data Manager
Primary FocusMonitoring trial sites for risks and complianceManaging and ensuring accuracy of trial data
Required SkillsMonitoring protocols, regulatory knowledge, site managementData management, database systems, quality control
Work EnvironmentClinical sites, monitoring visits, remote oversightData centers, clinical trial databases, office setting
CertificationsGCP, monitoring certificationsCDMP, data management certifications

While both roles are integral to clinical trials, Risk Based Monitoring focuses on overseeing site performance and compliance to mitigate risks, whereas Data Managers concentrate on managing and validating trial data for accuracy and integrity.

What are popular job titles related to Clinical Trial Risk Based Monitoring jobs in Austin, TX?

For Clinical Trial Risk Based Monitoring jobs in Austin, TX, the most frequently searched job titles are:

What job categories do people searching Clinical Trial Risk Based Monitoring jobs in Austin, TX look for?

The top searched job categories for Clinical Trial Risk Based Monitoring jobs in Austin, TX are:

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Cities near Austin, TX with the most Clinical Trial Risk Based Monitoring job openings:

Clinical Trial Risk Based Monitoring jobs near you
Infographic showing various Clinical Trial Risk Based Monitoring job openings in Austin, TX as of August 2026, with employment types broken down into 1% As Needed, 75% Full Time, 18% Part Time, and 6% Contract. Highlights an 87% Physical, 3% Hybrid, and 10% Remote job distribution, with an average salary of $82,438 per year, or $39.6 per hour.

Clinical Research Associate

Neuralink

Austin, TX • On-site

Full-time

Posted 25 days ago

Job description

Team Description:

The Neuralink Clinical team is at the heart of an ecosystem that merges neuroscience, engineering, and medicine. We work to shape the future of brain-computer interface (BCI) technology through the planning, launch, and execution of groundbreaking human clinical trials. Our team is built on a foundation of excellence, aiming to uphold the highest standards of Good Clinical Practice (GCP) while redefining what's possible and revolutionizing the way people interact with technology. Through strict compliance with ethical and regulatory protocols, we focus on ensuring the well-being of our trial participants while advancing the frontiers of neuroscience! Every day will bring fresh challenges and unprecedented opportunities to pioneer new approaches in the pursuit of our mission. From navigating regulatory pathways, designing trial protocols and documentation, and executing clinical trials, our team is instrumental in translating Neuralink's BCI technology for use in people!

Job Description and Responsibilities:

As a Clinical Research Associate, you'll play a crucial role in pioneering groundbreaking clinical studies. Your work will directly contribute to the planning, execution, and success of innovative trials, from the initial phases of study setup to hands-on clinical monitoring and site management. You'll be visiting sites both in-person and remotely to ensure protocol and regulatory compliance, tackle safety event management, and maintain essential documentation. Collaborating closely with a passionate, cross-functional team, as well as external partners, you'll be at the forefront of Neuralink's mission to push the boundaries of what's possible in clinical research. Additional job responsibilities will include:

  • Conduct site initiation, interim monitoring, and close-out visits (remote and on-site)
  • Ensure clinical studies are conducted in accordance with protocol, GCP, ISO 14155, and applicable regulatory requirements (e.g., 21 CFR Part 812)
  • Verify the accuracy, completeness, and consistency of clinical trial data through source data verification (SDV) and source data review (SDR)
  • Monitor participant safety by reviewing adverse events (AEs), serious adverse events (SAEs), and device deficiencies for completeness and timeliness
  • Ensure sites maintain adequate regulatory documentation, including Investigator Site Files (ISF), informed consent forms, and essential documents
  • Track site performance, enrollment, and data quality metrics; proactively identify risks and implement mitigation strategies
  • Support site training on protocol, investigational device use, and study procedures
  • Collaborate cross-functionally with Clinical Operations, Data Management, Regulatory, and Quality teams
  • Ensure timely resolution of data queries and protocol deviations
  • Prepare and maintain monitoring reports and follow-up letters in accordance with timelines
  • Support audit and inspection readiness at the site level

Required Qualifications:

  • Bachelor's degree in life sciences, engineering, or related field
  • 5+ years of clinical research experience (device experience strongly preferred)
  • Working knowledge of GCP (ICH E6), ISO 14155, and applicable FDA regulations
  • Experience with electronic data capture (EDC) systems and clinical trial documentation
  • Strong understanding of clinical trial processes, including monitoring and site management
  • Excellent communication, organization, and problem-solving skills
  • Ability to work independently in a fast-paced, evolving environment
  • Up to 30% travel (domestic and occasional international)

Preferred Qualifications:

  • Experience in neuromodulation, implantable devices, or other Class III medical devices
  • Experience supporting IDE or PMA clinical studies
  • Familiarity with risk-based monitoring approaches
  • Exposure to early feasibility or first-in-human studies
  • Exposure to market approval studies
  • Willingness and ability to travel up to 30-50% (domestic and occasional international)

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