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Clinical Data Engineer Jobs in Connecticut (NOW HIRING)

Actalent

Clinical Data Coordinator

New Haven, CT

$28 - $31.83/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Job Title: Clinical Data Coordinator We are seeking a Clinical Data Coordinator to join the ... About Actalent Actalent is a global leader in engineering and sciences services and talent ...

Actalent

Clinical Data Coordinator

New Haven, CT ยท On-site

$28 - $31.83/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Job Title: Clinical Data Coordinator๏ปฟ We are seeking a Clinical Data Coordinator to join the ... About Actalent Actalent is a global leader in engineering and sciences services and talent ...

Cooper Companies

Data Engineer Lead- PMS & QA

Trumbull, CT ยท On-site +1

  • Medical

  • Retirement

  • PTO

We currently offer over 600 clinically relevant medical devices to healthcare providers, including ... The Data Engineer Lead - PMS & QA leads data analysis, visualization, and reporting of Medical ...

CooperCompanies

Data Engineer Lead- PMS & QA

Trumbull, CT ยท On-site

  • Medical

  • Retirement

  • PTO

We currently offer over 600 clinically relevant medical devices to healthcare providers, including ... The Data Engineer Lead - PMS & QA leads data analysis, visualization, and reporting of Medical ...

Oxbridge Health

Senior Backend Engineer

Norwalk, CT ยท On-site

Data and Healthcare Standards * Work with structured and semi-structured healthcare data (for example, eligibility, claims, and clinical data). * Partner with Analytics and Data Engineering to ensure ...

CooperCompanies

Data Engineer Lead- PMS & QA

Trumbull, CT ยท On-site

  • Medical

  • Retirement

  • PTO

We currently offer over 600 clinically relevant medical devices to healthcare providers, including ... The Data Engineer Lead - PMS & QA leads data analysis, visualization, and reporting of Medical ...

Hyperfine

Clinical Scientist

Guilford, CT

$128K - $147K/yr

PhD or equivalent degree in biomedical engineering, neuroscience, imaging science, or related field * 2-5+ years of experience in clinical research, imaging, or data science in industry setting

Hyperfine

Clinical Scientist

Guilford, CT ยท On-site

$128K - $147K/yr

PhD or equivalent degree in biomedical engineering, neuroscience, imaging science, or related field * 2-5+ years of experience in clinical research, imaging, or data science in industry setting

Hyperfine

Clinical Scientist

Guilford, CT

$128K - $147K/yr

PhD or equivalent degree in biomedical engineering, neuroscience, imaging science, or related field * 2-5+ years of experience in clinical research, imaging, or data science in industry setting

Spire Orthopedic Partners

BI Engineer

Stamford, CT

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

... other clinical providers and 40 locations in New York, Connecticut, Rhode Island and Massachusetts. What you'll do: The Data Engineer will help build and support the data foundation that powers ...

ORTHOPAEDIC & NEUROSURGERY SPECIALISTS P.C.

BI Engineer

Stamford, CT ยท On-site +1

$113K - $169K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

... other clinical providers and 40 locations in New York, Connecticut, Rhode Island and Massachusetts. What you'll do: The Data Engineer will help build and support the data foundation that powers ...

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Showing results 1-20

All JobsClinical Data Engineer JobsClinical Data Engineer Jobs in Connecticut

Clinical Data Engineer information

See Connecticut salary details

$42.3K

$123.4K

$168.9K

How much do clinical data engineer jobs pay per year?

As of Aug 17, 2026, the average yearly pay for clinical data engineer in Connecticut is $123,397.00, according to ZipRecruiter salary data. Most workers in this role earn between $108,900.00 and $130,800.00 per year, depending on experience, location, and employer.

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

AspectClinical Data EngineerData Analyst
Required CredentialsBachelor's in Computer Science, Bioinformatics, or related field; knowledge of databases and programmingBachelor's in Statistics, Mathematics, or related field; proficiency in data visualization and analysis tools
Work EnvironmentHealthcare settings, research institutions, biotech companiesBusiness, healthcare, or research organizations across various industries
Employer & Industry UsageUsed in clinical research, healthcare IT, and pharmaceutical industriesUsed broadly in finance, marketing, healthcare, and other sectors

Clinical Data Engineers focus on building and maintaining data systems specific to clinical and healthcare data, requiring technical skills in databases and programming. Data Analysts interpret data to generate insights, often using visualization tools. While both roles handle data, Clinical Data Engineers are more technical and infrastructure-oriented, whereas Data Analysts focus on analysis and reporting.

What is a clinical data engineer?

A Clinical Data Engineer is a professional who designs, develops, and manages systems and processes for collecting, storing, and analyzing clinical trial or healthcare data. They work with large datasets, often using programming and database management skills, to ensure data integrity, quality, and security. Clinical Data Engineers collaborate with clinical researchers, data managers, and IT teams to streamline data workflows and support regulatory compliance. Their work is essential for enabling accurate analysis and reporting in clinical studies and improving healthcare outcomes.

What are the key skills and qualifications needed to thrive as a clinical data engineer, and why are they important?

To thrive as a Clinical Data Engineer, you need a strong background in data management, database design, and clinical data standards, often supported by degrees in computer science, health informatics, or related fields. Familiarity with tools such as SQL, Python, EDC systems (like Medidata or Oracle Clinical), and certifications in data handling or clinical research are typically required. Attention to detail, analytical thinking, and strong communication skills are essential soft skills for collaborating across clinical and technical teams. These skills ensure accurate data integration, regulatory compliance, and effective support for clinical research and decision-making.

How does a clinical data engineer typically collaborate with clinical research teams during a clinical trial?

Clinical Data Engineers work closely with clinical research teams to ensure that data collected during trials is accurate, secure, and accessible. They often design and maintain data pipelines, troubleshoot data integration issues, and provide technical support to clinical staff. Regular meetings with data managers, biostatisticians, and clinical coordinators help align technical solutions with study protocols and regulatory requirements. This collaborative environment ensures that data-driven insights can be generated efficiently and reliably throughout the study lifecycle.

What are popular job titles related to Clinical Data Engineer jobs in Connecticut?

For Clinical Data Engineer jobs in Connecticut, the most frequently searched job titles are:

What job categories do people searching Clinical Data Engineer jobs in Connecticut look for?

The top searched job categories for Clinical Data Engineer jobs in Connecticut are:

Clinical Data Engineer jobs near you
Infographic showing various Clinical Data Engineer job openings in Connecticut as of August 2026, with employment types broken down into 50% Full Time, and 50% Part Time. Highlights an 100% In-person job distribution, with an average salary of $123,397 per year, or $59.3 per hour.

AD, Principal Clinical Data Engineer

Boehringer Ingelheim Pharmaceuticals, Inc

Ridgefield, CT โ€ข On-site

Other

Posted 3 days ago

New

Job description

Description
Key contact partner in cultivating the "power of data" by means of (i) data collection/curation, data review, data delivery, (ii) data standardization or (iii) process definition, testing and training. Translate the science into technical specifications. Collect, ingest, structure, curate and standardize all kinds of Clinical Trial related data from internal and external sources. Ensure Data Quality and Integrity by implementing plausibility checks, anomaly detection, and fraud detection methods in data collection systems, with a strong focus on ensuring SDTM compliance, traceability, and readiness for regulatory submission. Supports the clinical research development process through the provision of advanced expertise in the areas of (i) data collection/curation, data review, delivery (ii) data standardization or (iii) process definition, testing and training.Possesses strong expertise in CDISC standards, particularly SDTM, including the ability to design, implement, review, and govern SDTM mapping specifications, datasets, and transformations to ensure regulatory-compliant data structures. This position interprets scientific/clinical requirements to translate and document them into Therapeutic Area/Project level technical specifications for new substances, indications or marketing claims.
As an employee of Boehringer Ingelheim, you will actively contribute to the discovery, development and delivery of our products to our patients and customers. Our global presence provides opportunity for all employees to collaborate internationally, offering visibility and opportunity to directly contribute to the companies' success. We realize that our strength and competitive advantage lie with our people. We support our employees in a number of ways to foster a healthy working environment, meaningful work, mobility, networking and work-life balance. Our competitive compensation and benefit programs reflect Boehringer Ingelheim's high regard for our employees.
Duties & Responsibilities
  • Accountable/Responsible to interpret requirements to translate and document them into project/TA level technical specifications. Provision clinical project/ TA level data to business consumers. Facilitate requirements gathering from consumers and develop global solutions to meet immediate and long-term needs of the business. Monitor and maintain ongoing project/ TA level operations of clinical data environments and respond to project/TA issues.
  • Leads and oversees all CDE tasks performed by an external partner. Oversees CRO capacities/budget for outsourced trial/project tasks.
  • Develop/test different ways to constantly improve data reliability, integrity and quality. Ensures real-time inspection readiness of all data collection, data review/data delivery (DBL) deliverables for a trial/project and participates in regulatory agency and BI internal audits as necessary.
  • Collaborate with/influence members of the development team within BDS and with neighboring colleagues at BI on the project/product goals. Contributes to cross-functional- and team-based thinking.
  • Keep abreast of data science and in particular new data collection/curation/standardization/digital tech solutions and innovative processes/tools within and outside BI. Turn derived insights into new CDE approaches relevant for clinical development, registration, and marketing of drugs.
  • Conduct and support data collection/curation/standards process & tool trainings for Clinical Data Engineers.
  • Participate in or Lead cross-functional BI internal process development teams and drive/plan relevant CDE (data collection/curation/standardization) aspects. Participate in external working groups.

Requirements
  • Bachelor's degree from an accredited institution, in Life Sciences, Computer Science, Software/Computer Engineering, or similar preferred, with many (greater than or equal to seven (>/= 7)) years of professional experience; Or
  • Master's degree (e.g. MBA, MSc) from an accredited institution, in Life Sciences, Computer Science, Software/Computer Engineering, or similar preferred, with greater than or equal to three (3) years of professional experience.
  • Initial experience within the pharmaceutical industry, CROs or academic sites.
  • Leadership experience required.
  • Broad knowledge and advanced experience in understanding of clinical trial development process required.
  • In-depth knowledge and experience with the use of Data Collection Tools (EDC systems), Data Review Tools, and/or Data Standardization methods, requirements
  • Thorough knowledge/experience in design of clinical trials, basic medical terminology and on processing clinical trial information.
  • Demonstrated ability to build/test, curate, oversee and interpret data in complex clinical trial and in projects with established BI experience.
  • Intellectual curiosity to find new and unusual ways solving data collection / curation / standardization / process definition, testing and training issues.
  • Excellent organizational skills, problem solving abilities, negotiation skills, time management skills and initiative required.
  • Strong communication skills: Confident and persuasive communicator to ensure that the message is clear and well understood.
  • Ability to work collaboratively on multi-disciplinary project teams and proactively manage relationships with external vendors required.
  • Mindful of local, global, internal and external cultures to ensure that messages are received positively and effectively.
  • Ability to lead and facilitate meetings required.
  • Ability to develop and deliver (technical) training required.
  • Language skills: English: fluent (Read/Write/Speak).
  • Know, understand, and implement:
    • International regulations and guidelines for good clinical and statistical practice from all ICH regions
    • The various international guidelines on clinical development, data standardization, and
    • BI processes and SOPs that govern clinical development in particular with respect to strategic areas (e.g. Clinical Development Plan)

Compensation
This position offers a base salary typically between $140,000 and $222,000. The position may be eligible for a role specific variable or performance based bonus and or other compensation elements. For an overview of our benefits please click here .

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