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Clinical Trial Risk Based Monitoring Jobs in Boston, MA

Clinovo

Clinical Trial Manager

Cambridge, MA · On-site

$175K/yr

The Clinical Trial Manager (CTM) plays a key role in the successful execution of clinical research ... monitoring activities, and risk mitigation efforts. * Evaluate vendor deliverables, performance ...

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 ...

Vor Bio

Senior/Clinical Trial Manager (CTM)

Boston, MA · On-site

$175K - $195K/yr

Conduct project risk analysis and develops risk mitigation strategies for a variety of complex ... CRF, monitoring plans, regulatory submission documents, clinical study report, investigator ...

Frontier Medicines

Clinical Trial Manager

Boston, MA · Hybrid

$120K - $150K/yr

This is a hybrid role based in our Boston, MA office, with an expectation of 2-3 days per week ... Monitor study performance metrics, timelines, and deliverables, and review CRO trip reports for ...

Lumicell

Senior Clinical Trial Manager

Waltham, MA · On-site

Develop and manage study timelines, milestones, risk mitigation plans, and site activation ... Maintain oversight of study progress, enrollment, data quality, monitoring team, compliance, and ...

Lumicell

Senior Clinical Trial Manager

Waltham, MA

Develop and manage study timelines, milestones, risk mitigation plans, and site activation ... Maintain oversight of study progress, enrollment, data quality, monitoring team, compliance, and ...

ARTBIO

Senior Clinical Trial Manager

Cambridge, MA · On-site +1

Perform clinical research site activities, which can include onsite or remote monitoring, co ... Ability to work independently, plan, prioritize, and risk mediate in a fast-paced environment.

Frontier Medicines

Clinical Trial Manager

Boston, MA · On-site

$120K - $150K/yr

This is a hybrid role based in our Boston, MA office, with an expectation of 2-3 days per week ... Monitor study performance metrics, timelines, and deliverables, and review CRO trip reports for ...

Frontier Medicines

Clinical Trial Manager

Boston, MA · On-site

$120K - $150K/yr

This is a hybrid role based in our Boston, MA office, with an expectation of 2-3 days per week ... Monitor study performance metrics, timelines, and deliverables, and review CRO trip reports for ...

AbbVie

Clinical Research Associate II

Boston, MA · On-site +1

$84K/yr

Focus on site clinical research that ensures appropriate conduct of the trial while driving ... Familiar with risk-based monitoring approach, onsite and offsite monitoring. * Knowledge of ...

Lumicell

Senior Clinical Trial Manager

Waltham, MA · On-site

Develop and manage study timelines, milestones, risk mitigation plans, and site activation ... Maintain oversight of study progress, enrollment, data quality, monitoring team, compliance, and ...

Vor Bio

Senior/Clinical Trial Manager (CTM)

Boston, MA · On-site

Conduct project risk analysis and develops risk mitigation strategies for a variety of complex ... Individual pay may vary based on multiple factors including but not limited to relevant job-related ...

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All JobsClinical Trial Risk Based Monitoring JobsClinical Trial Risk Based Monitoring Jobs in Boston, MA

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 22, 2026, the average hourly pay for clinical trial risk based monitoring in Boston, MA is $43.44, according to ZipRecruiter salary data. Most workers in this role earn between $35.00 and $47.79 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 Boston, MA?

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

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

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

What cities near Boston, MA are hiring for Clinical Trial Risk Based Monitoring jobs?

Cities near Boston, MA with the most Clinical Trial Risk Based Monitoring job openings:

Clinical Trial Risk Based Monitoring jobs near you

Clinical Trial Manager

Clinovo

Cambridge, MA • On-site

$175K/yr

Other

Posted 12 days ago

Job description

The Clinical Trial Manager (CTM) plays a key role in the successful execution of clinical research studies, providing operational leadership from study initiation through final closeout. This position is well-suited for a highly organized professional who excels in a collaborative environment, proactively addresses challenges, and thrives in a growing, fast-paced biotechnology setting. The CTM will manage relationships with CROs and vendors, oversee study timelines and budgets, and ensure that clinical trials are conducted efficiently, compliantly, and with a high standard of quality.
Key Responsibilities
Clinical Trial Planning & Management
  • Contribute to study planning activities, including protocol implementation, startup efforts, site feasibility, selection, and activation in partnership with Clinical Operations leadership.
  • Support the creation, review, and maintenance of essential study documentation, including protocols, informed consent forms, study manuals, and training materials.
  • Ensure clinical studies comply with applicable regulations, ICH-GCP standards, and internal procedures throughout the study lifecycle.
CRO & Vendor Management
  • Act as the primary operational liaison for contract research organizations (CROs) and external service providers.
  • Monitor study progress, including site performance, patient enrollment, monitoring activities, and risk mitigation efforts.
  • Evaluate vendor deliverables, performance indicators, and quality metrics, identifying and escalating concerns when necessary.
Clinical Operations Leadership
  • Assist with management of study budgets, timelines, forecasting activities, and support the development of contracts and statements of work.
  • Facilitate cross-functional study team meetings and promote effective communication among Clinical Development, Biostatistics, Data Management, Safety, Regulatory Affairs, and other stakeholders.
  • Support inspection readiness initiatives and participate in audit responses, corrective actions, and process improvements.
Data Management & Quality Oversight
  • Collaborate with Data Management teams to support database development, data review, query resolution, and data cleaning activities.
  • Review clinical data outputs, protocol deviations, and safety-related documentation to ensure quality and compliance.
  • Maintain complete, accurate, and inspection-ready Trial Master File (TMF) documentation.
Study Closeout Activities
  • Coordinate site closure activities, reconciliation processes, and final study deliverables.
  • Contribute to Clinical Study Report (CSR) development and capture lessons learned to support continuous improvement initiatives.
Qualifications
  • Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related discipline; advanced degree preferred.
  • Minimum of 5 years of clinical operations experience within the biotechnology, pharmaceutical, or clinical research industry, including direct management of clinical studies.
  • Strong knowledge of clinical trial operations, ICH-GCP guidelines, regulatory requirements, and vendor oversight practices.
  • Prior experience working in startup, small biotechnology, or growth-stage organizations is highly desirable.
  • Demonstrated ability to manage multiple projects simultaneously, identify risks early, and work independently while collaborating effectively with senior leadership.
  • Excellent project management, communication, organizational, and cross-functional leadership skills.
  • Proven ability to build productive partnerships with internal teams, investigators, CROs, and external vendors.

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