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Clinical Research Data Engineer Jobs (NOW HIRING)

Dana-Farber Cancer Institute

The Research Data Specialists will support the clinical research program in the areas of data collection, computing, and database organization. Duties include the examination, synthesis, and ...

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Clinical Research Data Engineer information

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$37K

$106K

$142.5K

How much do clinical research data engineer jobs pay per year?

As of Jun 8, 2026, the average yearly pay for clinical research data engineer in the United States is $106,012.00, according to ZipRecruiter salary data. Most workers in this role earn between $104,000.00 and $104,000.00 per year, depending on experience, location, and employer.

What is the difference between Clinical Research Data Engineer vs Clinical Data Analyst?

AspectClinical Research Data EngineerClinical Data Analyst
Required CredentialsBachelor's or higher in computer science, bioinformatics, or related field; knowledge of data engineering toolsBachelor's or higher in life sciences, statistics, or related field; proficiency in data analysis software
Work EnvironmentData infrastructure development, database management, coding in SQL, Python, or RData interpretation, reporting, statistical analysis, visualization
Employer & Industry UsagePharmaceutical companies, CROs, biotech firms focusing on data pipeline setupClinical research organizations, hospitals, biotech firms analyzing trial data

The Clinical Research Data Engineer primarily focuses on building and maintaining data infrastructure for clinical trials, while the Clinical Data Analyst interprets and reports on the data collected. Both roles require strong data skills but differ in technical focus and daily tasks.

Research Intern

Research Intern

Tranquil Clinical Research

Webster, TX

Other

Posted 8 days ago

Job description

Please do not call our office - we will reach out to you.
Description
The Research Intern is an entry level clinical research position. The Intern will perform a variety of research, database and clerical duties of a routine and technical nature to support clinical trials and assist investigators to organize, gather and compile clinical research data. The Intern will primarily be responsible for the collection, aggregation, and analysis of data. The Research Intern will also form other duties such as data entry, and administrative duties such as filing, record keeping, photocopying, and creating flyers/posters. The Research Intern will be supervised by a senior research staff member or principal investigator.
Qualifications
Minimum Education
High School Diploma or GED (Required) Or
Bachelor's Degree May require a Bachelor's degree based on the specific internship program
Minimum Work Experience
0-2 years related experience. 2 years experience working in a medical or scientific research setting, preferred
Required Skills/Knowledge
Demonstrates adherence with the standards for the responsible conduct of research.
Work requires organizational skills, knowledge of basic mathematical, data collection and analysis, and research principles.
Knowledge of human subjects research.
Excellent computer skills in a Windows and/or Mac environment.
Excellent writing, editing, and proofing skills.
Required Licenses and Certifications
CITI Certification (Required)
Valid Driver's license
Functional Accountabilities
Research Projects

  • Maintain confidentiality of data, as required.
  • Plan, conduct and manage research projects.
  • Responsible for appropriate use of research funds and resources.
Project Administration
  • Ensure compliance with program guidelines and requirements of funding and regulatory agencies.
  • Stay informed of and adhere to human research protection guidelines, relevant best practices, and changes to any research protocol.
  • Accurately complete IRB submissions on time.
  • Anticipate study needs and work to accomplish them in a timely manner.
  • Seek assistance, when needed.
Data Collection
  • Collect data in order to facilitate operational and clinical research activities.
  • Enter clinical and research data and information into database, include electronic CRFs and sample tracking databases.
  • Follow established guidelines in the collection of clinical data and/or administration of clinical studies.
  • Support aggregation and analysis of study data, as directed by senior research staff.
Professional Development
  • Attend and contribute to team meetings, including working to set and achieve project timelines and deliverables.
  • Obtain training and certification as required by study protocol (e.g., CITI training).
  • Comply with all annual job-related training requirements.

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