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Clinical Research Data Abstractor Jobs in Springfield, MA

Connecticut Children's

Research Assistant 2

Hartford, CT · On-site

$19.50 - $26.75/hr

Ensures data integrity, quality control and compliance with all protocols associated with assigned ... clinical activities associated with conducting research for assigned research project(s)

Connecticut Children's

Research Assistant 2

Hartford, CT · On-site

$19.50 - $26.75/hr

Ensures data integrity, quality control and compliance with all protocols associated with assigned ... clinical activities associated with conducting research for assigned research project(s)

Connecticut Children's

Research Assistant 2

Hartford, CT · On-site

$19.50 - $26.75/hr

Ensures data integrity, quality control and compliance with all protocols associated with assigned ... clinical activities associated with conducting research for assigned research project(s)

Connecticut Children's

Research Assistant 2

Hartford, CT · On-site

$19.50 - $26.75/hr

Ensures data integrity, quality control and compliance with all protocols associated with assigned ... clinical activities associated with conducting research for assigned research project(s)

IQVIA

Clinical Trial Rater

Springfield, MA · Remote

... clinical research services. We collaborate with top pharmaceutical and biotech companies to accelerate innovation and improve patient outcomes. Our mission is to combine data science and human ...

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All JobsClinical Research Data Abstractor JobsClinical Research Data Abstractor Jobs in Springfield, MA

Clinical Research Data Abstractor information

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$43

$62

How much do clinical research data abstractor jobs pay per hour?

As of Aug 30, 2026, the average hourly pay for clinical research data abstractor in Springfield, MA is $43.98, according to ZipRecruiter salary data. Most workers in this role earn between $36.15 and $52.21 per hour, depending on experience, location, and employer.

What is a clinical research data abstractor?

A Clinical Research Data Abstractor is a professional responsible for collecting and extracting important data from medical records, clinical trials, or patient charts. They ensure that the data is accurate, complete, and entered into research databases or electronic systems. This role is vital in supporting clinical research studies by ensuring high-quality data for analysis, compliance, and reporting. Clinical Research Data Abstractors often work closely with research coordinators, physicians, and other healthcare professionals.

What skills and qualifications are needed to be a clinical research data abstractor?

To thrive as a Clinical Research Data Abstractor, you need strong attention to detail, knowledge of medical terminology, and experience with data collection, often supported by a degree in health sciences or a related field. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and possibly certifications like ACRP-CP or SoCRA-CCRP is common. Excellent organizational skills, critical thinking, and the ability to communicate clearly with research teams help set top performers apart. These skills ensure accurate, timely data abstraction that is vital for regulatory compliance and the integrity of clinical research studies.

What are common challenges faced by clinical research data abstractors, and how can they be managed?

Clinical Research Data Abstractors often encounter challenges such as interpreting complex medical records, ensuring data accuracy, and navigating various electronic health record (EHR) systems. To manage these challenges, it's helpful to develop strong attention to detail, maintain up-to-date knowledge of medical terminology, and collaborate closely with clinical teams for clarification when needed. Additionally, frequent communication with data managers and adhering to standardized data abstraction protocols can greatly reduce errors and improve data quality.

What is the difference between Clinical Research Data Abstractor vs Clinical Research Coordinator?

AspectClinical Research Data AbstractorClinical Research Coordinator
Primary RoleExtracts and summarizes data from clinical trial recordsManages overall study operations and participant coordination
Required SkillsAttention to detail, data management, basic medical knowledgeRegulatory compliance, patient interaction, study oversight
Work EnvironmentData entry labs, clinical trial sites, research officesClinical sites, hospitals, research institutions
CertificationsTypically none required, but certifications like CCR can helpOften requires CCRC or similar certifications

While both roles support clinical research, the Clinical Research Data Abstractor focuses on data extraction and analysis, whereas the Clinical Research Coordinator manages study logistics and participant interactions. Understanding these differences helps in choosing the right career path or job search focus.

What job categories do people searching Clinical Research Data Abstractor jobs in Springfield, MA look for?

The top searched job categories for Clinical Research Data Abstractor jobs in Springfield, MA are:

What cities near Springfield, MA are hiring for Clinical Research Data Abstractor jobs?

Cities near Springfield, MA with the most Clinical Research Data Abstractor job openings:

Clinical Research Data Abstractor jobs near you
Infographic showing various Clinical Research Data Abstractor job openings in Springfield, MA as of August 2026, with employment types broken down into 1% As Needed, 82% Full Time, 14% Part Time, and 3% Contract. Highlights an 84% Physical, 4% Hybrid, and 12% Remote job distribution, with an average salary of $91,476 per year, or $44 per hour.

Clinical Research Data Assistant - Oncology

Trinityhealth

Hartford, CT • On-site

Full-time

Posted 5 days ago

Job description

Employment Type:Full timeShift:Day ShiftDescription:Trinity Health Of New England is seeking a detail-oriented Clinical Research Data Assistant to support our growing Oncology Clinical Research Program. This role is responsible for the accurate collection, management, analysis, and reporting of clinical research data to ensure compliance with study protocols, regulatory requirements, and sponsor expectations.
The Research Data Assistant serves as a key member of the research team, collaborating closely with Clinical Research Coordinators, investigators, healthcare providers, and external sponsors to maintain data integrity throughout the lifecycle of oncology clinical trials. Success in this role requires exceptional organizational skills, strong analytical abilities, attention to detail, and the ability to manage multiple studies and deadlines simultaneously.
This position offers an opportunity to contribute directly to advancing cancer research and improving patient outcomes while working within a mission-driven healthcare organization.

What You Will Do

  • Collect, review, and enter study data from medical records, laboratory reports, source documents, and other approved data sources into protocol-specific databases.
  • Ensure timely completion of case report forms (CRFs) and resolution of data queries within sponsor-defined timelines.
  • Evaluate source documentation for accuracy, completeness, and protocol compliance.
  • Maintain study databases and monitor participant follow-up activities to support ongoing and long-term clinical trials.
  • Utilize multiple data platforms including electronic health records and research systems to identify, track, and analyze participant data.
  • Support implementation of Trinity Health, Trinity Health Of New England, and Institutional Review Board (IRB) policies and procedures.
  • Partner with Clinical Research Coordinators, study investigators, and healthcare providers to obtain and verify required study data.
  • Assist with tracking, processing, and shipment of biological specimens, including blood and tissue samples, as required by study protocols.

Minimum Qualifications

  • Bachelor's degree preferred; equivalent combination of education and relevant experience will be considered.
  • Experience in a clinical healthcare setting along with working knowledge of oncology medical terminology and electronic medical records is required.
  • Previous clinical research, research coordination, or data management experience preferred.
  • Experience navigating EPIC is required. Experience with research databases such as Medidata Rave, REDCap, and EPIC SlicerDicer preferred.

Position Highlights and Benefits

  • Full Time, 40 Hours, Days
  • Great benefits from Day 1
  • Patient-centric environment
  • Career growth and advancement potential

Why Join Trinity Health Of New England?

At Trinity Health Of New England, our colleagues are dedicated to advancing compassionate care, innovative research, and improved patient outcomes. As part of our Oncology Clinical Research team, you will play a meaningful role in supporting groundbreaking cancer research and helping bring new treatment options to patients throughout our communities. Be at the forefront of advancing oncology research while making a difference in the lives of patients and families every day.

Our Commitment

Rooted in our Mission and Core Values, we honor the dignity of every person and recognize the unique perspectives, experiences, and talents each colleague brings. By finding common ground and embracing our differences, we grow stronger together and deliver more compassionate, person-centered care. We are an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or any other status protected by federal, state, or local law.

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