ZipRecruiter

Log In

1

Clinical Trial Risk Based Monitoring Jobs in Massachusetts

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

$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 · 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 ...

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 ...

previous pagenext page

Showing results 21-40

All JobsClinical Trial Risk Based Monitoring JobsClinical Trial Risk Based Monitoring Jobs in Massachusetts

Clinical Trial Risk Based Monitoring information

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 Massachusetts?

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

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

The top searched job categories for Clinical Trial Risk Based Monitoring jobs in Massachusetts are:

What cities in Massachusetts are hiring for Clinical Trial Risk Based Monitoring jobs?

Cities in Massachusetts 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 Massachusetts as of August 2026, with employment types broken down into 86% Full Time, and 14% Part Time. Highlights an 100% In-person job distribution.

Clinical Trial Manager

Kymera Therapeutics

Watertown, MA • On-site

$115K - $200K/yr

Full-time

Re-posted 17 days ago

Job description

Who we are:
Kymera is a clinical-stage biotechnology company pioneering the field of targeted protein degradation (TPD) to develop medicines that address critical health problems and have the potential to dramatically improve patients' lives. Kymera is deploying TPD to address disease targets and pathways inaccessible with conventional therapeutics. Having advanced the first degrader into the clinic for immunological diseases, Kymera is focused on building an industry-leading pipeline of oral small molecule degraders to provide a new generation of convenient, highly effective therapies for patients with these conditions. Founded in 2016, Kymera has been recognized as one of Boston's top workplaces for the past several years. For more information about our science, pipeline and people, please visit www.kymeratx.com or follow us on X (formerly Twitter) or LinkedIn.
How we work:
  • PIONEER: We are courageous, resilient and rigorous in our mission to improve patients' lives through our revolutionary degrader medicines.
  • COLLABORATE: We value trust + transparency from everyone. Our goals are shared, our decisions data-driven and our camaraderie genuine.
  • BELONG: We recognize our differences, inviting curiosity and inclusivity, so that our people are valued, seen, and heard.

How you'll make an impact:
  • Contribute to the planning, implementation and execution of a global clinical trial
  • Responsible for management of vendors to support clinical trial execution
  • Plan, execute, and lead study-specific meetings (e.g., internal core team meetings, investigator meetings, etc), as needed
  • Provide input for the design of the Informed Consent Form(s), eCRFs, monitoring conventions, edit checks, etc.
  • Provide study-specific training and leadership to clinical research staff, CRO, CRAs, sites and other contract personnel.
  • Manage study timelines and metrics to ensure completion of study deliverables
  • Support site selection, qualification, initiation, and monitoring activities.
  • Review monitoring reports to ensure quality and resolution of site-related issues.
  • Ensure timely enrollment and data collection at clinical trial sites.
  • Collaborate with the data management team to ensure data integrity and timely database lock.
  • Review and analyze clinical trial data to identify trends and potential issues.
  • Ensure tracking and review of protocol deviations and assess impact on study data
  • Develop relationships with investigators and site staff
  • Work closely with CRO and Medical Monitor to ensure safety and efficacy data appropriately summarized to facilitate review.
  • Work closely with translational medicine team to ensure appropriate incorporation of bioanalytical sampling plan into clinical protocols and relevant data output of the trial is provided to functional groups for review.
  • Maintain accurate and complete trial documentation.
  • Proactively identify and resolve clinical project issues

Skills and experience you'll bring:
  • Bachelor of Science in Life Sciences and 3+ years (CTM)/5+ years (Sr. CTM) as a project/clinical trial manager in biotech/pharmaceutical industry.
  • Experience working on large, global, complex Phase 2 clinical trial(s).
  • Broad knowledge of regulatory and ICH GCP guidelines, HIPAA, Protection of Human Research Subjects.
  • Strong project management skills with the ability to manage multiple trials simultaneously.
  • Excellent problem-solving, leadership, and communication skills.
  • Ability to work in a fast-paced, dynamic environment with cross-functional teams.

Equal Employment Opportunity
Kymera Therapeutics is proud to be an equal opportunity employer, seeking to create a welcoming and diverse environment. All applicants will receive consideration for employment without regard to race, color, religion, creed, gender, national origin, age, disability, veteran status, pregnancy, sex, marital status, gender expression or identity, genetic information, sexual orientation, citizenship, or any other legally protected class.
Compensation
  • Kymera offers a competitive compensation package that recognizes both results and capabilities through market-based, performance-driven pay.
  • The anticipated base salary range for this role is $115,000 - $200,000, with eligibility for annual bonus, equity participation, and comprehensive benefits.
  • Actual salary is based on a holistic evaluation of the specific role/level as well as each candidate's depth of experience and the capabilities they bring to the position.

Apply