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Clinical Trial Risk Based Monitoring Jobs in Boston, MA

Candel Therapeutics

Clinical Trial Associate

Needham, MA · On-site

$88K - $100K/yr

The Clinical Trial Associate (CTA) role supports clinical trial execution in Ph 2 and Ph 3 trials ... This could include a review of monitoring reports and source document review. * Maintain study ...

Candel Therapeutics

Clinical Trial Associate

Needham, MA · On-site

$88K - $100K/yr

The Clinical Trial Associate (CTA) role supports clinical trial execution in Ph 2 and Ph 3 trials ... This could include a review of monitoring reports and source document review. * Maintain study ...

Biogen

Clinical Trial Manager

Cambridge, MA · Hybrid

$117K - $157K/yr

This is a hybrid role to be based at our Headquarters in Cambridge, MA. What You'll Do: * Support ... Monitor study progress and operational metrics, identifying and escalating risks or issues ...

Prometrika LLC

Clinical Trial Associate II

Cambridge, MA · On-site

$75K - $90K/yr

The Clinical Trial Associate II (CTA II) supports, coordinates, and implements clinical research ... May assist with reviewing monitoring visit reports The CTA II will also perform the following CTA ...

Skyhawk Therapeutics

Clinical Trial Associate

Waltham, MA · On-site

$75K - $140K/yr

Lab Manual, site flowcharts). * Assist with monitoring trip report across the program. Requirements ... Skyhawk Therapeutics will assess the appropriate level for a qualified candidate based on job ...

IQVIA

Clinical Trial Rater

Boston, MA · Remote

Clinical Trial Rater - Borderline Personality Disorder (BPD) Location ... Remote based in the US Hours: Approximately 5h per week Role: Clinical Specialist Start: immediate ...

Alpha-9 Oncology

Clinical Trial Manager

Boston, MA

Support tracking of clinical trial timelines, budgets, key operational metrics, and study risks ... Review study site monitoring reports in alignment with the CRO oversight plan. * Responsible for ...

Skyhawk Therapeutics

Clinical Trial Associate

Waltham, MA · On-site

$75K - $140K/yr

Lab Manual, site flowcharts). * Assist with monitoring trip report across the program. Requirements ... Skyhawk Therapeutics will assess the appropriate level for a qualified candidate based on job ...

Alpha-9 Oncology

Clinical Trial Manager

Boston, MA · On-site

Support tracking of clinical trial timelines, budgets, key operational metrics, and study risks ... Review study site monitoring reports in alignment with the CRO oversight plan. * Responsible for ...

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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 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

Kailera Therapeutics, Inc.

Waltham, MA • On-site

$127K - $155K/yr

Full-time

Medical, Life, Retirement

Posted 18 days ago

Job description

At Kailera, we are bold, authentic and committed to our mission of developing therapies that give people the power to transform their lives and elevate their overall health. Rooted in an entrepreneurial spirit and a team-oriented culture, we are working together to advance Kailera's mission to advance novel therapies for obesity and related conditions.
We are passionate about creating an inclusive workplace that promotes collaboration, integrity, and excellence. As we expand, we seek the most talented individuals with diverse backgrounds, cultures, perspectives, and experiences to join our team.
What You'll Do:
The Clinical Trial Manager will provide project support to team members by leading and/or participating in the daily management of clinical trial activities. Successful candidate will be working closely with and will be responsible for oversight of study activities through our CROs and service providers, including study start-up, conduct, and completion.
This position provides an opportunity to join a rapidly growing Clinical Operations organization and contribute substantially to the building of the department and the successful implementation of trials.
Required location: Waltham, MA (hub-based, onsite 3-4 days per week)
Responsibilities:
  • Perform as the lead interface with the CRO regarding status of project activities and deliverables (including but not limited to site identification and selection, pre-study activities, enrollment, management/conduct, database lock, post-study activities)
  • Collaborate with the cross-functional clinical trial team to review and prepare various clinical study documents including but not limited to study protocol, model informed consent forms, and study plans
  • Lead day-to-day management of external vendors, as needed, to support the trial design and implementation
  • Review and approve internal and external vendor study plans and processes, as applicable
  • Review monitoring reports and interact with CRO to ensure the quality of monitoring and site management
  • Work with cross-functional team to ensure data query management and data retrieval is taking place in a timely manner
  • Review deviation listings and site audit reports and work with team to resolve site issues (e.g., staff retraining, additional resources)
  • Maintain and ensure the quality and completeness of study master files in compliance with GCP
  • Lead Clinical Study Team meetings internally, and/or with CRO and service providers

Required Qualifications:
  • Work experience to include a minimum of 6 years clinical trial experience with a solid understanding of functional area responsibilities associated with the clinical development process
  • Good working knowledge of ICH-GCP guidelines and regulatory requirements for clinical trial management
  • Must have strong clinical study management, communication (oral and written), and analytical skills
  • Excellent interpersonal skills, with a demonstrated ability to work in a team environment as well as independently
  • Additional attributes include an ability to multi-task, be flexible, and to thrive in a fast-paced environment
  • Demonstrated ability to effectively manage external vendors & CROs
  • Advanced proficiency in Microsoft Office and Microsoft Project or other Project Management software
  • Demonstrated strong written and verbal communication skills
  • Must be able to travel

Education:
  • BA/BS; Life Science degree a plus

Salary Range
$127,000-$155,000 USD
For Full Time Roles: This range represents the company's good-faith estimate of the salary at the time of posting. Actual pay may vary based on experience, skills, qualifications, location, and internal equity. We also offer comprehensive health coverage, flexible time off, paid holidays, and a year-end shutdown. Enjoy a monthly wellness stipend, generous 401(k) match, tuition reimbursement, commuter benefits, disability and life insurance, plus annual bonus opportunities and equity grants-because your well-being and future matter to us.
EQUAL EMPLOYMENT OPPORTUNITY INFORMATION:
Kailera Therapeutics, Inc. is an Equal Opportunity Employer that does not discriminate on the basis of actual or perceived race (including traits historically associated with race, such as hair texture and protective hairstyles), color, creed, religion (including religious dress and grooming practices), national origin, ancestry, citizenship status, age (40 and over), sex or gender (including pregnancy, childbirth, pregnancy-related conditions, and lactation), gender identity or expression (including transgender status), sexual orientation, marital status, military service and veteran status, physical or mental disability, genetic information, reproductive health decisions, domestic victim status, political affiliation, or any other characteristic protected by applicable federal, state, or local laws and ordinances.
E-Verify:
Kailera Therapeutics, Inc. uses E-Verify to confirm the identity and employment eligibility of all new hires.
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