Clinical Trial Data Coordinator – Boston, Massachusetts

Job Description

About the Company

SkillGigs is a global IT and healthcare consulting firm that connects skilled professionals with leading organizations worldwide. This opportunity is with one of our U.S.-based healthcare and research partners, focused on advancing clinical research, ensuring data integrity, and supporting innovative treatment development.

Job Title:

Clinical Trial Data Coordinator

Location:

Boston

Job Overview

We are seeking a detail-oriented Clinical Trial Data Coordinator to support the collection, management, and validation of clinical trial data. In this role, you will ensure data accuracy, maintain compliance with research protocols, and collaborate with clinical and research teams. This position is ideal for individuals interested in clinical research, data management, and healthcare innovation.

Key Responsibilities
Collect, review, and manage clinical trial data from various sources
Ensure accuracy, completeness, and consistency of research data
Maintain and update clinical trial databases and systems
Verify data against source documents and resolve discrepancies
Ensure compliance with clinical trial protocols and regulatory requirements
Collaborate with investigators, coordinators, and research teams
Prepare reports and documentation for audits and reviews
Support data queries and data cleaning activities
Maintain confidentiality and data security standards
Assist in monitoring study progress and timelines
Required Qualifications
Bachelor’s degree in Life Sciences, Healthcare, or related field
2–4 years of experience in clinical research or data coordination
Strong knowledge of clinical trial processes and data management
Familiarity with Good Clinical Practice (GCP) guidelines
Experience with clinical data management systems (CDMS)
Strong analytical and attention-to-detail skills
Good communication and organizational abilities
Preferred Qualifications
Experience in clinical trial coordination or research data management
Familiarity with electronic data capture (EDC) systems
Certification in clinical research (e.g., CCRC, CCRP)
Knowledge of regulatory requirements (FDA, ICH guidelines)
Strong problem-solving and data validation skills
Why Join Us?
Opportunity to work with a leading U.S.-based research organization
Hands-on experience in clinical trials and data management
Supportive and collaborative work environment
Competitive salary and benefits package
Career growth opportunities in clinical research
How to Apply

We recommend submitting an ATS-friendly resume highlighting your experience in clinical research, data management, and regulatory compliance. Including certifications and measurable achievements will strengthen your application.