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Clinical Trial Risk Based Monitoring Jobs in Massachusetts

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 ...

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 ...

IQVIA

Clinical Trial Rater

Springfield, 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 ...

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 ...

Galderma

Senior Clinical Trial Manager

Boston, MA · On-site

$110K - $135K/yr

The Opportunity The Senior Clinical Trial Manager (CTM) plans and manages overall activities for ... Work environments and physical requirements may vary based on the requirements of the role.

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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 Associate

Candel Therapeutics

Needham, MA • On-site

$88K - $100K/yr

Full-time

Re-posted 7 days ago

Job description

  • Location: Hybrid, Needham, MA 

  • Salary:  $88k-$100k  

Why Work With Us?   
At Candel, our people drive our success. We value diversity, collaboration, and bold thinking in a supportive, mission-driven environment. Like a team, we show up for each other and stay focused on making a difference for patients and families. Our leadership is transparent and empowering, and our culture is built on trust, flexibility, and accountability, encouraging ownership and innovation every day.   

Our Science: Advancing Cancer Immunotherapies   
Candel is a clinical-stage biopharma company developing off-the-shelf, multimodal immunotherapies that stimulate personalized, systemic anti-tumor responses. Our platforms use genetically modified adenovirus and HSV constructs. With positive Phase 3 results for our lead candidate, it’s an exciting time to join us and help bring transformative cancer treatments to patients. Learn more: www.candeltx.com   

Position Summary: 

The Clinical Trial Associate (CTA) role supports clinical trial execution in Ph 2 and Ph 3 trials. This role includes working on multiple protocols with the potential to cross-train across different oncology indications using a variety of clinical trial databases. 

Essential Areas of Responsibility: 

  • Execute and support day-to-day clinical trial operations in alignment with protocols, timelines, and regulatory requirements.  

  • Participate in reviewing, formatting, and finalizing study-related templates, logs, plans, and manuals and ongoing training of personnel. 

  • Assist in collecting and completing essential study-related activities, including data entry into multiple databases. 

  • Ensure the quality of data submitted from assigned study tasks and timely data submission, including appropriate progress reporting. 

  • Manage imaging vendor and maintain tracking of invoices, sample delivery and recovery from the vendor site. 

  • Assist in the planning and organizing study-specific meetings and write and distribute regular updates. 

  • Assist the Clinical Trial Manager in select site management activities. This could include a review of monitoring reports and source document review. 

  • Maintain study-related trackers that will support Clinical Operations and individual studies. 

  • Perform primary review of submitted clinical data, database entry, and source document verification according to established standard operating procedures (SOPs). 

  • participate in the review and verification of data for quality control processes. 

  • Ensure quality in documentation and archiving of clinical data. 

  • Support invoice tracking, purchase order coordination, and budget-related activities for study. 

Minimum Education, Experience and Skill Requirements: 

Education: 

  • Bachelor’s degree in a health-related discipline or similar.  

Experience: 

  •  At least 2 years of experience in the clinical research/pharmaceutical/biotech arena and an understanding of clinical research and the requirements of a clinical operations function. 

  • Excellent verbal and written communication skills, good organizational and interpersonal skills, and team drive. 

  • Knowledge of GCP and FDA regulations related to clinical trial conduct and familiarity with industry best practices. 

  • Able to manage multiple projects independently and use varying databases and management systems. 

  • Discretion in handling confidential information. 

  • Knowledge of project management tools and practices and proficiency in using normal office software: Microsoft Word, Excel, and PowerPoint. 

Must be authorized to work in US. We cannot provide sponsorships. 
 
*** NOTE: We are not accepting resumes from agencies. *** 

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