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Remote Director Data Engineering Jobs in Connecticut

Milliman

Strategic Data Partnership Manager

Windsor, CT · Remote

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

This position is fully remote, while occasional travel may be required. Primary Responsibilities ... You'll work closely with product, engineering, legal, sales and other market-facing teams. * Grow ...

Cigna

Director, Technical Product Management - Applied AI

Bloomfield, CT · On-site +1

$232K - $243K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Working across Finance, Engineering, Data, and Architecture teams, this leader translates complex ... Open to remote if not aligned to office location with a strong preference East Coast. If you will ...

Arvinas

  • Medical

  • Dental

  • Vision

  • Life

Arvinas uses its proprietary PROTAC ® Discovery Engine platform to engineer proteolysis targeting ... This role can be located at our headquarters in New Haven, CT or work with a hybrid or remote work ...

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Infographic showing various Remote Director Data Engineering job openings in Connecticut as of August 2026, with employment types broken down into 1% As Needed, 84% Full Time, 12% Part Time, and 3% Contract. Highlights an 83% Physical, 4% Hybrid, and 13% Remote job distribution.

Technical Clinical Data Manager /Data Analyst (Remote)

Penfield Search Partners

Fairfield, CT • Remote

Full-time

Posted 16 days ago

Job description

Contact: Neisha Camacho/Terra Parsons -
No 3rd party candidates

We are partnering with a growing biotech organization seeking a Clinical Data Manager/Data Analyst to support ongoing and upcoming clinical programs across multiple therapeutic areas.

This role will sit within a highly collaborative clinical development team and is ideal for a hands-on, analytical Clinical Data Manager who enjoys digging into the data, identifying trends or issues proactively, and developing creative solutions to improve data quality and study execution. The client is seeking someone resourceful and technically curious — not just process-oriented — with the ability to independently explore datasets, generate meaningful reports, and surface potential issues early.

The ideal candidate will bring a blend of traditional clinical data management expertise along with strong data review, querying, and analytical skills. Experience with R, SQL, SAS, or other data interrogation and reporting tools is highly desirable.

Key Responsibilities

  • Support clinical data management activities across studies from start-up through database lock
  • Perform hands-on data review and exploratory analysis to identify data trends, inconsistencies, missing data patterns, and potential study risks
  • Develop custom reports, listings, and data visualizations to support proactive data cleaning and study oversight
  • Utilize R, SQL, SAS, or similar tools to query, analyze, and troubleshoot clinical datasets
  • Partner with CROs and vendors to ensure high-quality, timely data delivery
  • Collaborate cross-functionally with Clinical Operations, Biostatistics, Statistical Programming, Medical, and Safety teams on data review strategies and issue resolution
  • Contribute to development and review of key deliverables including:
    • Data Management Plans (DMPs)
    • eCRF design and completion guidelines
    • Edit checks and query logic
    • User Acceptance Testing (UAT)
    • Data review plans and cleaning processes
  • Support ongoing query management and ensure data integrity, consistency, and inspection readiness
  • Assist with implementation of data standards, reporting enhancements, and process improvements
  • Work independently to investigate data anomalies and recommend practical solutions in a fast-paced biotech environment

Qualifications

  • BS in a scientific, technical, or clinical discipline
  • Approximately 5–8 years of clinical data management experience within biotech, pharma, or CRO environments
  • Strong hands-on experience reviewing and interrogating clinical trial data
  • Experience using R, SQL, SAS, or other querying/reporting tools to analyze clinical data and generate custom reports
  • Experience with EDC systems such as Medidata Rave, Oracle, or Veeva
  • Working knowledge of CDISC standards (SDTM/ADaM) and downstream data usage
  • Experience supporting Phase II and/or III clinical trials; CNS experience is a plus
  • Exposure to CRO/vendor oversight
  • Understanding of clinical data structures and dictionaries including MedDRA and WHODrug
  • Strong critical thinking and problem-solving skills with the ability to work independently
  • Resourceful, proactive, detail-oriented, and comfortable operating in a dynamic biotech environment
  • Strong communication and cross-functional collaboration skills