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Clinical Trial Risk Based Monitoring Jobs (NOW HIRING)

Ardelyx

In House Clinical Research Associate

Newark, CA · On-site

$99K - $121K/yr

Partner with Clinical Trial Managers and CRO monitoring teams to provide sponsor oversight and ensure monitoring activities align with the study's risk-based monitoring strategy * Track and analyze ...

Ardelyx

In House Clinical Research Associate

Newark, CA · On-site +1

$99K - $121K/yr

Partner with Clinical Trial Managers and CRO monitoring teams to provide sponsor oversight and ensure monitoring activities align with the study's risk-based monitoring strategy * Track and analyze ...

Ardelyx

In House Clinical Research Associate

Waltham, MA · On-site +1

$99K - $121K/yr

Partner with Clinical Trial Managers and CRO monitoring teams to provide sponsor oversight and ensure monitoring activities align with the study's risk-based monitoring strategy * Track and analyze ...

Ardelyx

In House Clinical Research Associate

Waltham, MA · On-site +1

$99K - $121K/yr

Partner with Clinical Trial Managers and CRO monitoring teams to provide sponsor oversight and ensure monitoring activities align with the study's risk-based monitoring strategy * Track and analyze ...

Ardelyx

In House Clinical Research Associate

Waltham, MA · On-site +1

$99K - $121K/yr

Partner with Clinical Trial Managers and CRO monitoring teams to provide sponsor oversight and ensure monitoring activities align with the study's risk-based monitoring strategy * Track and analyze ...

Prometrika LLC

Clinical Trial Manager

Cambridge, MA · On-site

$140K - $168K/yr

... site monitoring oversight, clinical vendor management, clinical trial risk management, TMF ... management, and regulatory submissions (e.g., CSR, NDA support). * Experience working in cross ...

Kymera Therapeutics

Clinical Trial Manager

Watertown, MA · On-site

$115K - $200K/yr

Review monitoring reports to ensure quality and resolution of site-related issues. * Ensure timely ... Actual salary is based on a holistic evaluation of the specific role/level as well as each ...

Ossium Health

Clinical Trial Manager

San Francisco, CA · On-site +1

$145K - $165K/yr

... monitoring. You'll play a key role in launching our PRESERVE II clinical trial, the long-term ... This position is based in our San Francisco office; we maintain a hybrid schedule of Monday ...

Kymera Therapeutics

Clinical Trial Manager

Watertown, MA · On-site

$115K - $200K/yr

Review monitoring reports to ensure quality and resolution of site-related issues. * Ensure timely ... Actual salary is based on a holistic evaluation of the specific role/level as well as each ...

4D Molecular Therapeutics

Clinical Trial Manager

Experience reviewing trial plans including developing creative strategies for site monitoring, risk mitigation, trial budgets, site selection, and clinical supplies management * Clinical research ...

Ardelyx

Clinical Trial Manager

Waltham, MA · On-site +1

$136K - $160K/yr

... Monitoring Plans, Laboratory Manuals, Patient Diaries, Clinical Site Procedures Manual and CRF ... Implement risk management and mitigation strategies, prioritizing tasks and issues to ensure ...

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

As of May 31, 2026, the average hourly pay for clinical trial risk based monitoring in the United States is $39.99, according to ZipRecruiter salary data. Most workers in this role earn between $32.21 and $43.99 per hour, depending on experience, location, and employer.

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.

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 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 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.

More about Clinical Trial Risk Based Monitoring jobs
What cities are hiring for Clinical Trial Risk Based Monitoring jobs? Cities with the most Clinical Trial Risk Based Monitoring job openings:
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Clinical Trial Risk Based Monitoring jobs near you
Infographic showing various Clinical Trial Risk Based Monitoring job openings in the United States as of May 2026, with employment types broken down into 4% As Needed, 81% Full Time, 5% Part Time, 2% Temporary, 7% Contract, and 1% Nights. Highlights an 92% Physical, 6% Hybrid, and 2% Remote job distribution, with an average salary of $83,169 per year, or $40 per hour.
In House Clinical Research Associate

In House Clinical Research Associate

Ardelyx

Newark, CA • On-site

$99K - $121K/yr

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 3 days ago

Job description

Description
Ardelyx is a commercial-stage biopharmaceutical company focused on redefining treatment approaches for patients with significant unmet medical needs. By combining scientific innovation with a collaborative, purpose-driven culture, we strive to create meaningful impact for patients.
Team Ardelyx is united by a shared mission and guided by our core values: Passionate, Fearless, Dedicated, and Inclusive.
We foster an inclusive environment where employees are respected, supported, and empowered to make an impact - both within our company and in the lives of patients we serve.
Position Summary:
The Clinical Research Associate (CRA) supports sponsor oversight of clinical trial execution with an focus on site performance, data quality, and regulatory compliance. Building on prior experience in a Clinical Trial Assistant (CTA) or similar role, the CRA II independently manages assigned sites and supports study oversight of clinical trial execution.
This role partners closely with Clinical Trial Managers, Field CRAs, vendors, and cross-functional stakeholders to ensure trials are conducted in accordance with ICH-GCP, applicable regulations, and internal governance standards. The CRA II contributes to proactive risk identification, issue resolution and continuous inspection readiness.
Responsibilities:
  • Provide sponsor oversight of assigned investigative sites, serving as the primary operational and ensuring high - quality protocol execution, and compliance with GCP, and regulatory requirements
  • Monitor site performance through centralized and remote review of study data, key performance metrics, and monitoring outputs, including proactively identify and escalate issues with recommended mitigation strategies
  • Support study start-up, conduct, and close-out activities, including site feasibility, activation, training, and close-out documentation
  • Ensure timely collection, review, and maintenance of essential regulatory documents and maintain Trial Master File (TMF) completeness, quality and inspection readiness
  • Partner with Clinical Trial Managers and CRO monitoring teams to provide sponsor oversight and ensure monitoring activities align with the study's risk-based monitoring strategy
  • Track and analyze protocol deviations, safety events, data discrepancies, and site performance trends; collaborate with cross-functional teams to drive timely resolution
  • Support regulatory and inspection readiness by overseeing IRB/EC submissions and approvals, maintaining accurate site documentation, and contributing to audit and inspection preparation, responses, and follow-up activities
  • Collaborate cross-functionally with Clinical Operations, Data Management, Safety, Regulatory Affairs, and Biostatistics, and support sponsor oversight of CROs and other
  • Participate in investigator meetings, study team meetings, and internal governance as required

Qualifications:
  • Bachelor's degree in relevant scientific discipline with 2-5 years of experience in clinical research, clinical operations or healthcare-related roles or equivalent combination of education and experience
  • Prior experience as a Clinical Trial Assistant (CTA), Study Coordinator, or similar clinical research role required
  • Working knowledge of ICH-GCP, FDA regulations, and global clinical trial requirements
  • Experience with sponsor systems EDC, eTMF, CTMS and centralized monitoring tools
  • Strong analytical skills with the ability to interpret study and site-level performance trends
  • Excellent written and verbal communication skills with high level of attention to detail
  • Demonstrated sponsor mindset with a focus on quality, accountability, and compliance
  • Ability to work independently while escalating issues appropriately
  • Strong problem abilities and proactive risk identification skills
  • Effective collaboration and stakeholder management abilities
  • Thrives in a collaborative environment and enjoys working cross-functionally to solve operational challenges.
  • Ability to travel as needed

The anticipated annualized base pay range for this full-time position is $99,000 - $121,000. Ardelyx utilizes industry data to ensure that our compensation is competitive and aligned with our industry peers. Actual base pay will be determined based on a variety of factors, including years of relevant experience, training, qualifications, and internal equity. The compensation package may also include an annual bonus target and equity awards, subject to eligibility and other requirements.
Ardelyx also offers a robust benefits package to employees, including a 401(k) plan with generous employer match, 12 weeks of paid parental leave, up to 12 weeks of living organ and bone marrow leave, equity incentive plans, health plans (medical, prescription drug, dental, and vision), life insurance and disability, flexible time off, annual Winter Holiday shut down, and at least 11 paid holidays.
Ardelyx is an equal opportunity employer.

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