Clinical Trial Data Processing Assistant – Springfield, Massachusetts

April 28, 2026
$14 - $33 / hour
Urgent
Application ends: May 22, 2026
Apply Now

Job Description

About the Company
SkillGigs is an advanced talent marketplace connecting skilled healthcare and technology professionals with leading organizations across the United States. This opportunity is with one of our trusted U.S.-based healthcare and life sciences partners, focused on clinical research, data management, and trial operations.
Job Overview
We are seeking a detail-oriented and analytical professional to support clinical trial data processing initiatives. In this role, you will assist with clinical data entry, trial documentation, data validation, and regulatory compliance to ensure the accuracy and integrity of clinical research operations.
Key Responsibilities

Process and manage clinical trial data in electronic data capture (EDC) systems

Review patient and study data for completeness and accuracy

Support data cleaning, validation, and discrepancy resolution

Maintain trial documentation and regulatory compliance records

Coordinate with clinical research teams, sponsors, and data managers

Assist with case report forms (CRFs) and trial reporting requirements

Track study milestones and generate data processing reports

Ensure adherence to GCP, FDA, and HIPAA standards

Support quality assurance and audit readiness initiatives

Contribute to efficient clinical trial workflow and data integrity

Required Qualifications

Bachelor’s degree in Life Sciences, Healthcare Administration, Public Health, Clinical Research, or related field

1–3 years of experience in clinical research, healthcare data processing, or medical administration

Basic understanding of clinical trial operations and data management processes

Familiarity with medical terminology and regulatory documentation

Strong analytical, organizational, and communication skills

Detail-oriented with problem-solving capabilities

Preferred Qualifications

Experience with EDC systems, CTMS, or clinical research software

Knowledge of GCP, FDA regulations, HIPAA, and research compliance standards

Familiarity with clinical trial protocols and study coordination

Basic understanding of biostatistics or research data analysis

Relevant certifications such as CCRC, CCRP, or clinical research credentials

Why Join Us?

Work with a leading U.S.-based healthcare and life sciences organization through SkillGigs

Gain hands-on experience in clinical research and trial data management

Supportive and collaborative professional environment

Competitive salary and benefits

Career growth opportunities in clinical operations, healthcare data, and research management

How to Apply
Submit an ATS-friendly resume highlighting your experience in clinical data management, research coordination, healthcare systems, regulatory compliance, and relevant certifications.