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Clinical Data Management Associate Jobs in Connecticut

Zimmer Biomet

$15 - $20/hr

What You Can Expect The Clinical Applications Intern is responsible for providing support to the Biostatistics & Clinical Data Management (BCDM) department in the development and maintenance of ...

Zimmer Biomet

$15 - $20/hr

What You Can Expect The Clinical Applications Intern is responsible for providing support to the Biostatistics & Clinical Data Management (BCDM) department in the development and maintenance of ...

Zimmer Biomet

$15.25 - $20.25/hr

What You Can Expect The Clinical Applications Intern is responsible for providing support to the Biostatistics & Clinical Data Management (BCDM) department in the development and maintenance of ...

Zimmer Biomet

$15.25 - $20.25/hr

What You Can Expect The Clinical Applications Intern is responsible for providing support to the Biostatistics & Clinical Data Management (BCDM) department in the development and maintenance of ...

Zimmer Biomet

$15.25 - $20.50/hr

What You Can Expect The Clinical Applications Intern is responsible for providing support to the Biostatistics & Clinical Data Management (BCDM) department in the development and maintenance of ...

Zimmer Biomet

$16 - $21.25/hr

What You Can Expect The Clinical Applications Intern is responsible for providing support to the Biostatistics & Clinical Data Management (BCDM) department in the development and maintenance of ...

Pwc

Data Strategy-Manager

Stamford, CT

$99K - $232K/yr

... Management Professional) - Informatica Certified Professional - Alation Certified Data Catalog Professional - Collibra Certified Ranger/Steward/Expert - SAP Certified Application Associate - SAP ...

Pwc

Data Strategy-Manager

Hartford, CT

$99K - $232K/yr

... Management Professional) - Informatica Certified Professional - Alation Certified Data Catalog Professional - Collibra Certified Ranger/Steward/Expert - SAP Certified Application Associate - SAP ...

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Showing results 21-40

All JobsClinical Data Management Associate JobsClinical Data Management Associate Jobs in Connecticut

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 11, 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:
Clinical Data Management Associate jobs near you

Clinical Research and Data Coordinator

The Fertility Partners US

Norwalk, CT • On-site

$75K - $95K/yr

Full-time

Re-posted 9 days ago

Job description

Overview:
The Clinical Research and Data Coordinator supports clinical trials and research studies by coordinating daily study operations, managing participant interactions, maintaining regulatory documentation, and ensuring accurate collection and reporting of research data. This role works closely with laboratory staff, investigators, and multidisciplinary teams to support successful study completion and compliance with research standards.

Responsibilities:

  • Coordinate daily activities for clinical research studies, including participant scheduling, study visits, documentation, and follow-up.
  • Assist with preparation and maintenance of clinical research documents, including protocols, informed consent forms, case report forms, study materials, and IRB submissions.
  • Recruit, screen, and educate potential study participants on study requirements, procedures, risks, benefits, and expectations.
  • Conduct participant interviews, obtain informed consent, and ensure adherence to study protocols and ethical guidelines.
  • Monitor participant progress, document study-related observations, and communicate concerns or updates to the research team.
  • Collect, enter, verify, and maintain accurate clinical research data while performing regular quality checks and audits.
  • Maintain electronic records, regulatory files, meeting documentation, and study-related correspondence.
  • Collaborate with clinical teams, investigators, and administrative staff to ensure timely completion of research milestones.
  • Support data reporting activities, including preparation of summaries, tracking reports, and research documentation.
  • Assist with staff training, protocol updates, process improvements, and additional research initiatives as needed.

Qualifications:

  • Bachelor’s degree in healthcare, business administration, life sciences, or related field.
  • 1–2+ years of administrative, project coordination, or clinical research experience preferred.
  • Experience with human clinical research, IRB processes, or regulatory documentation strongly preferred.
  • Strong organizational skills with the ability to manage multiple priorities and deadlines.
  • Excellent written and verbal communication skills.
  • Detail-oriented with strong problem-solving and critical-thinking abilities.
  • Proficiency with Microsoft Office and electronic data management systems.

About the Role:
The ideal candidate is a motivated, organized professional who can work independently while collaborating with a multidisciplinary team to support high-quality research and patient experiences.