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

As of Aug 16, 2026, the average hourly pay for clinical trial risk based monitoring in Maple Grove, MN is $40.94, according to ZipRecruiter salary data. Most workers in this role earn between $32.98 and $45.05 per hour, depending on experience, location, and employer.

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.

How to become a clinical trial risk based monitoring?

To become a clinical trial risk-based monitor, candidates typically need a bachelor's degree in life sciences, healthcare, or related fields, along with experience in clinical research or monitoring. Certification such as the Association of Clinical Research Professionals (ACRP) or Society of Clinical Research Associates (SoCRA) can enhance job prospects. Strong knowledge of Good Clinical Practice (GCP) guidelines and proficiency with electronic data capture (EDC) systems are also important.

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 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.

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 job categories do people searching Clinical Trial Risk Based Monitoring jobs in Maple Grove, MN look for?

The top searched job categories for Clinical Trial Risk Based Monitoring jobs in Maple Grove, MN are:

What cities near Maple Grove, MN are hiring for Clinical Trial Risk Based Monitoring jobs?

Cities near Maple Grove, MN with the most Clinical Trial Risk Based Monitoring job openings:

Clinical Trial Risk Based Monitoring jobs near you

Senior Clinical Research Scientist

Anteris Technologies

Eagan, MN • On-site

Full-time

Re-posted 28 days ago

Job description

Anteris® Technologies is a global structural heart company dedicated to revolutionizing cardiac care. With offices in Minneapolis, MN, US; Geneva, Switzerland; and Brisbane and Perth, Australia, we have a growing and inclusive team.

Our mission is to forge new frontiers in cardiac care by pioneering science-driven and measurable advancements to restore heart valve patients to healthy function. Transcatheter Aortic Valve Replacement (TAVR) technologies were originally designed for older, high-risk patients. Today, younger, more active patients need a better solution that will not just open and close but restore healthy heart function. We seek to restore healthy blood flow patterns by creating the world's first biomimetic TAVR valve, DurAVR® THV. This cutting-edge valve, incorporating our proprietary ADAPT® anti-calcification technology, is designed to mimic the natural function of a healthy heart valve.

The Senior Clinical Research Scientist will provide scientific, clinical, and operational expertise to support Anteris' global clinical studies and ensure scientific objectives are achieved. This individual will work cross-functionally on the design, execution, monitoring, interpretation, and communication of clinical trial data to help advance patient outcomes through Anteris' breakthrough structural heart technologies.

This position reports to the Senior Manager, Clinical Research and collaborates closely with the broader clinical and cross-functional teams to support ongoing clinical studies, clinical documentation, and the dissemination of clinical data through publications and congress activities. This is a highly visible role with the opportunity to make a significant impact at Anteris Technologies.

At Anteris Technologies, you'll join a mission-driven team dedicated to improving the lives of patients with aortic stenosis through breakthrough structural heart technologies while helping shape the future of structural heart care.

Primary Duties and Responsibilities

  • Represent Anteris as an industry leader within scientific, clinical research, and industry organizations
  • Serve as a Scientific Lead and Subject Matter Expert for Anteris-sponsored clinical studies
  • Partner cross-functionally to support the scientific objectives of Anteris-sponsored clinical studies and advance the company's mission as a science-driven organization
  • Lead execution of the subject selection process to ensure accurate and timely review of subject eligibility criteria, with oversight from clinical leadership
  • Oversee external vendor performance and drive effective cross-functional collaboration
  • Contribute to clinical trial design, protocol development, protocol revisions, and reports supporting regulatory submissions, with guidance from clinical leadership
  • Participate in publication planning activities in collaboration with cross-functional stakeholders
  • Support charter development for clinical studies in partnership with external vendors and study leadership, with oversight from clinical leadership
  • Perform data analysis and interpretation in collaboration with external biostatisticians and internal data management teams
  • Deliver timely study updates to clinical and cross-functional leadership through clear, well-structured presentations and data summaries
  • Develop, maintain, and review clinical study reports and related documentation
  • Contribute to root cause analyses, corrective and preventive actions, and effectiveness monitoring, with oversight from clinical leadership
  • Collaborate with internal and external stakeholders, including study sites, vendors, and committees, to support clinical trial objectives and appropriately escalate issues when needed
  • Build and maintain strong relationships with study investigators and key opinion leaders
  • Contribute to Medical Legal Review (MLR) activities as a clinical subject matter expert for external data releases, ensuring scientific accuracy and appropriate clinical interpretation prior to publication or disclosure
  • Assist in compiling clinical documentation and data for regulatory submissions
  • Provide cross-functional clinical training and education support

Required Education & Experience

  • Advanced degree in Life Sciences required; MD or PhD preferred
  • 5+ years of Clinical Science or Clinical Research experience within cardiology, cardiovascular, or medical device environments
  • Experience contributing scientifically to medical device clinical trials
  • Proficiency in medical terminology and medical writing, including experience working within ICMJE guidelines
  • Knowledge of healthcare ethics and compliance regulations
  • Strong work ethic, self-motivation, collaboration skills, and excellent written and verbal English communication skills

Preferred Skills, Knowledge, Experience & Qualifications:

  • TAVR clinical research experience strongly preferred
  • Extensive clinical or scientific experience with advanced training in research, study design, and statistics (MSN, PhD, MS, or equivalent)
  • Experience with imaging modalities, including echocardiography, CT, and CMR interpretation
  • Experience supporting international, multi-center, randomized clinical trials
  • Experience with statistical software programs such as Matlab, SPSS, or SAS is a strong plus

What We Offer:

  • Opportunity to make a significant impact on the healthcare industry by advancing groundbreaking therapies.
  • Collaborative and dynamic work environment with a culture of innovation and excellence.
  • Competitive compensation package, including salary, performance-based bonuses, and stock options.
  • Career development opportunities and a chance to be part of a growing company that values its employees.

Health and Wellness Offerings:

  • Medical, Dental, and Vision Plans
  • Flexible Spending Account (FSA)
  • 401k + Company Match
  • Life, AD&D, Short-Term and Long-Term Disability Insurance
  • Bonus Plan Eligibility
  • Employee Stock Option Plan
  • Paid Holidays & Vacation
  • Employee Assistance Program
  • Inclusive Team Environment

This is the national market pay scale.

Salary Range
$130,000—$160,000 USD

Note: We may require proof of COVID-19 vaccination to comply with health institutions, state, local municipality, and/or travel regulations.

Anteris Technologies recruits, employs, trains, compensates, and promotes regardless of race, religion, color, national origin, sex, disability, age, veteran status, and other protected status as required by applicable law. We have a clear vision: to be a place of belonging for all humans by promoting diversity, multiculturism and inclusion, as a goal and reflection across the organization. Diversity is more than a commitment - it is part of our mission to deliver the best structural heart products on a global scale.