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Internship Clinical Research Informatics Jobs in Boston, MA

QUANTERIX CORP

Laboratory Informatics Analyst

Bedford, MA · On-site

$100K - $120K/yr

Laboratory Informatics Analyst (LIMS & Clinical Operations) Location: Bedford, MA Quanterix is a global leader in ultra-sensitive biomarker detection, enabling breakthroughs in disease research ...

Quanterix

Laboratory Informatics Analyst

Bedford, MA · Hybrid

$100K - $120K/yr

Laboratory Informatics Analyst (LIMS amp; Clinical Operations) Location: Bedford, MA Quanterix is a ... From discovery through clinical research, Akoya offers a full continuum of solutions, including ...

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All JobsClinical Research Informatics JobsInternship Clinical Research Informatics JobsInternship Clinical Research Informatics Jobs in Boston, MA

Internship Clinical Research Informatics information

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How much do internship clinical research informatics jobs pay per month?

As of Aug 29, 2026, the average monthly pay for internship clinical research informatics in Boston, MA is $6,995.92, according to ZipRecruiter salary data. Most workers in this role earn between $4,800.00 and $8,325.00 per month, depending on experience, location, and employer.

What is an internship in clinical research informatics?

An Internship in Clinical Research Informatics is a temporary position designed for students or recent graduates to gain hands-on experience in managing and analyzing data in clinical research settings. Interns typically work alongside experienced informaticians and researchers to support clinical trials, data management, and the development of health information systems. The role helps interns develop skills in data analysis, electronic health records, and research methodology. It is an ideal starting point for those interested in the intersection of healthcare, research, and information technology.

What types of projects or tasks can I expect to work on during an internship in clinical research informatics?

As a Clinical Research Informatics intern, you may be involved in tasks such as managing and analyzing clinical trial data, assisting with the development or optimization of electronic data capture systems, and supporting data quality assurance processes. Interns often collaborate closely with clinical research coordinators, data managers, and IT teams to ensure data integrity and regulatory compliance. You might also contribute to the design of study databases, help generate reports for ongoing studies, and participate in team meetings to discuss project progress. This role provides valuable exposure to both technical and clinical aspects of research, offering a strong foundation for future career growth in informatics or clinical research.

What are the key skills and qualifications needed to thrive as an intern in clinical research informatics?

To thrive in an Internship Clinical Research Informatics role, candidates typically need a background in life sciences or health informatics, basic understanding of clinical research methodologies, and strong analytical skills. Familiarity with data management tools, electronic data capture (EDC) systems, and statistical software like SAS or R is often expected. Attention to detail, effective communication, and a willingness to learn are valuable soft skills that help interns stand out. These skills are crucial for ensuring accurate data handling, supporting research teams, and contributing to successful clinical research outcomes.

What is the difference between Internship Clinical Research Informatics vs Clinical Data Analyst?

AspectInternship Clinical Research InformaticsClinical Data Analyst
Required CredentialsTypically pursuing or recent graduate in health informatics, life sciences, or related fieldsBachelor's or master's in health informatics, data science, or related areas
Work EnvironmentInternship setting within research institutions, hospitals, or pharmaceutical companiesHealthcare organizations, research institutions, or data-focused teams
Employer & Industry UsageUsed in academic, clinical research, and pharmaceutical sectors for training and entry-level rolesCommon in healthcare and research for analyzing clinical data and supporting decision-making

Internship Clinical Research Informatics focuses on training and gaining experience in managing clinical data and informatics systems, often as a stepping stone into the industry. Clinical Data Analysts primarily analyze and interpret clinical data to support research and healthcare decisions. Both roles involve working with health data but differ in experience level and focus.

What are the most commonly searched types of Clinical Research Informatics jobs in Boston, MA?

The most popular types of Clinical Research Informatics jobs in Boston, MA are:

Internship Clinical Research Informatics jobs near you
Infographic showing various Internship Clinical Research Informatics job openings in Boston, MA as of August 2026, with employment types broken down into 83% Full Time, and 17% Part Time. Highlights an 100% In-person job distribution, with an average salary of $83,951 per year, or $40.4 per hour.

Clinical Informatics Manager

Tango Therapeutics

Boston, MA • On-site

Full-time

Posted 3 days ago

New

Job description

Company Overview
Tango Therapeutics is a biotechnology company dedicated to discovering novel drug targets and delivering the next generation of precision medicine for the treatment of cancer.
Using an approach that starts and ends with patients, Tango leverages the genetic principle of synthetic lethality to discover and develop therapies that take aim at critical targets in cancer.
This includes expanding the universe of precision oncology targets into novel areas such as tumor suppressor gene loss and their contribution to the ability of cancer cells to evade immune cell killing.
The Tango labs and offices are located at 201 Brookline Avenue, in the Fenway area of Boston, Massachusetts.
Summary
Tango has an exciting new opportunity to join the Biometrics team as Clinical Informatics Manager. In this role you will report to the Vice President, Data Management. You will be a subject matter expert at Centralized Imaging, electronic Clinical Outcome Assessments (eCOA) and other clinical technologies from study start up through data generation, decommissioning, and documentation archival. Clinical technologies will encompass a spectrum of systems including but not limited to eCOA, IRT and Centralized imaging. This position will enable clinical data management and support clinical data issue resolution for these technologies, ensuring high-quality clinical data to support key initiatives. You will be forward-thinking about the needs of a clinical development operations organization and possess high attention to detail. You will maintain a collaborative outlook with the ability to pursue multiple options in parallel.
Your Role:
  • Serve as the Central Imaging, eCOA and clinical technologies Subject Matter Expert for Tango's clinical studies and programs
  • Lead clinical technologies including planning, execution, and delivery of the clinical data activities on Centralized Imaging, eCOA and clinical technologies, implementing secure procedures to initiate best practices and lead data management flow
  • Demonstrate strong technical expertise to maintain high standards of data integrity, accuracy, reliability, efficiency and compliance with regulatory requirements
  • Partnering closely with Clinical Data Management and Clinical Operations, assist with documentation and oversight of clinical data quality and timeliness such as tracking, KPIs, data management and monitoring
  • Lead cross-functional collaboration to gather requirements, design systems, and deliver technology solutions on time, ensuring data quality and compliance standards are consistently met.
  • Responsible for implementation project management, including clinical data systems integrations with EDC and reporting systems. Aid in device management as needed
  • Oversee facilitation of clinical technologies technical support, data changes, data issue resolution; working with cross-functional stakeholders including Clinical Data Management, Clinical Operations and Biostatistics in order to achieve goals
  • Responsible for user acceptance testing oversight and documentation, including UAT test case creation, facilitating signatures on documentation, and risk and impact assessment
  • Responsible for the administration and uploading of documentation to appropriate eTMF
  • Enable and guide study teams by delivering exceptional customer service and technical support for daily use of clinical systems.
  • May assist with process updates, cross-functional initiatives, standards documentation updates, and/or SOPs
  • Support inspection readiness activities as needed
  • Additional duties and responsibilities as required

What You Bring:
  • 7+ years of clinical systems experience in the pharmaceutical or biotech industry
  • Bachelor's degree in a science-based subject (advanced degree preferred)
  • eCOA and/or Centralized Imaging Subject Matter Expertise with an in depth understanding of clinical development process and regulatory frameworks governing solutions
  • Hands-on Data Management experience of EDC, eCOA, IRT and Centralized imaging
  • Experience with user requirement specifications/user test scripts with clinical data technologies
  • Prior demonstration of creative, capable problem solving and innovation as it relates to integrations between clinical systems (eCOA, IRT, EDC, etc.) in a clinical research environment
  • Prior engagement in activities that involve system development lifecycle to support the use of clinical technologies within a clinical study
  • Ability to deal with time demands, incomplete information and prioritize tasks
  • Technical excellence and solid technical skills across data platforms
  • Working knowledge of ICH, GAMP, FDA, IRB/IEC and other applicable regulations/guidelines and demonstrated understanding of clinical research protocol requirements and appropriate reporting of clinical trial data
  • Ability to work independently with a high level of attention and act with initiative to address issues
  • Flexible, team-oriented, ability to manage multiple projects in a fast-paced environment
  • Strong project management
  • Excellent written and oral communication skills
  • Demonstrated proficiency with MS Office, such as Outlook, Word, Excel, PowerPoint, and SharePoint

We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.
#LI-Hybrid
Salary range
$144,800-$217,200 USD

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