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Clinical Data Management Associate Jobs in Connecticut

Senior Clinical Data Manager

New Haven, CT · On-site

$133K - $173K/yr

  • Medical

  • Retirement

  • PTO

Oversee CRO data management counterparts for assigned clinical trials and ensure that the data management objectives are met in accordance with current SOPs, WPDs and timelines and budget. * Initiate ...

Senior Clinical Data Manager

New Haven, CT · On-site

$133K - $173K/yr

  • Medical

  • Retirement

  • PTO

Oversee CRO data management counterparts for assigned clinical trials and ensure that the data management objectives are met in accordance with current SOPs, WPDs and timelines and budget. * Initiate ...

Clinical Data Coordinator

New Haven, CT · On-site

$28 - $31.83/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

The coordinator will provide direct clinical and data management support related to the conduct of clinical trials and the collection and reporting of study-related clinical data for clinical studies ...

New

Clinical Data Coordinator

New Haven, CT

$28 - $31.83/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

The coordinator will provide direct clinical and data management support related to the conduct of clinical trials and the collection and reporting of study-related clinical data for clinical studies ...

New

About Bridgewater Bridgewater Associates is a premier asset management firm, focused on delivering ... About Your Role As a Data Associate, you will help us achieve our mission by owning and deeply ...

About Bridgewater Bridgewater Associates is a premier asset management firm, focused on delivering ... About Your Role As a Data Associate, you will help us achieve our mission by owning and deeply ...

Support GCM associates perform reconciliation tasks by comparing and analyzing the data from ... The global Case Management Associate in PSPV supports the reconciliation process for these sources ...

Clinical Research Data Coordinator

New Haven, CT · On-site

$32 - $35/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Manage multiple priorities and tasks independently while maintaining high standards of data quality ... Associate's or Bachelor's degree in Life Sciences, Healthcare, or a related field is preferred. * 3 ...

Database Associate

Milford, CT · On-site

$57K - $71K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

The Database Associate will be responsible for supporting database maintenance and security by ... Help ensure data security by managing access controls and user permissions. * Document processes ...

Co-lead establishment of a company-wide clinical trial data management and analytics platform* Develop future leaders by mentoring Clinical Scientists and associate clinical scientists across program ...

New

... clinical and data management support related to the conduct of clinical trials and the collection and reporting of study-related clinical data for clinical studies within the assigned disease team or ...

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Showing results 1-20

Clinical Data Management Associate information

See Connecticut salary details

$13

$37

$82

How much do clinical data management associate jobs pay per hour?

As of Aug 15, 2026, the average hourly pay for clinical data management associate in Connecticut is $37.05, according to ZipRecruiter salary data. Most workers in this role earn between $27.88 and $37.07 per hour, depending on experience, location, and employer.

What is the difference between Clinical Data Management Associate vs Clinical Data Coordinator?

AspectClinical Data Management AssociateClinical Data Coordinator
ResponsibilitiesData entry, validation, database management, ensuring data qualityOversees data collection, manages databases, coordinates data flow between teams
Required SkillsAttention to detail, knowledge of clinical data systems, basic understanding of regulationsStrong organizational skills, data management experience, communication skills
Work EnvironmentClinical research labs, CROs, pharmaceutical companiesClinical trial sites, research organizations, CROs
Common UsageEntry to mid-level data roles in clinical trialsData oversight and coordination roles in clinical studies

The Clinical Data Management Associate focuses on data entry, validation, and database management, ensuring data accuracy. The Clinical Data Coordinator oversees data collection and flow, coordinating between teams. Both roles require similar skills and work environments but differ in scope and responsibilities.

What are the most commonly searched types of Clinical Data Management jobs in Connecticut?

The most popular types of Clinical Data Management jobs in Connecticut are:

Technical Clinical Data Manager /Data Analyst (Remote)

Penfield Search Partners

Fairfield, CT • Remote

Full-time

Posted 15 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