Junior Clinical Data Coordinator

United Consulting Hub; United States; Remote; USD 30.000 - 39.000; Teilzeit

Zusammenfassung

United Consulting Hub, Inc. is seeking a Junior Clinical Data Coordinator for a remote contract role. You will support clinical research data management, review study information, and help maintain accurate electronic data records.

This position emphasizes data quality, adherence to GCP, and teamwork with study teams. Suitable for candidates with 0–2 years in clinical data management and strong attention to detail.

Qualifikationen

• Basic knowledge of clinical research, trials, data management, and medical terminology.
• Familiarity with EDC systems, CRFs, clinical databases, and Excel.
• Understanding of GCP, study documentation, data quality and confidentiality requirements.
• Ability to identify data discrepancies, maintain accurate records, and communicate effectively with research teams.
• Strong organizational, analytical, time management, and attention-to-detail skills.

Aufgaben

• Assist with collecting, entering, reviewing, and maintaining clinical trial data in EDC systems.
• Review study records, CRFs, and source documents to identify missing or incomplete information.
• Support data cleaning by identifying discrepancies and assisting with data queries.
• Maintain study trackers, data entry logs, and documentation per procedures.
• Coordinate with CRAs, investigators, and data management teams to obtain missing information.
• Assist with database review, data reconciliation, and preparation of data status reports.
• Follow GCP and established data management procedures.

Kenntnisse

Clinical data management

GCP knowledge

Microsoft Excel

Attention to detail

Communication with research teams

Tools

EDC systems

CRFs

Jobbeschreibung

Job Title: Junior Clinical Data Coordinator

Type: Contract

Location: Remote

Experience: 0–2 Years

Job Summary:

The Junior Clinical Data Coordinator supports clinical research and clinical trial data management activities. The role involves reviewing clinical study information, maintaining electronic data records, resolving basic data discrepancies, and supporting clinical research teams in maintaining accurate and reliable study data.

Key Responsibilities:

• Assist with collecting, entering, reviewing, and maintaining clinical trial data in electronic data capture (EDC) systems.
• Review clinical study records, case report forms (CRFs), and source documents to identify missing, inconsistent, or incomplete information.
• Support data cleaning activities by identifying discrepancies and assisting with the resolution of data queries.
• Maintain clinical study trackers, data entry logs, and documentation according to approved study procedures.
• Coordinate with clinical research associates, investigators, and data management teams to obtain missing or corrected study information.
• Assist with database review, data reconciliation, and preparation of clinical data status reports.
• Follow clinical research protocols, Good Clinical Practice (GCP), and established data management procedures.
• Maintain confidentiality and ensure appropriate handling of patient-related information throughout clinical data activities.

Skills Required:

• Basic knowledge of clinical research, clinical trials, clinical data management, and medical terminology.
• Familiarity with EDC systems, CRFs, clinical databases, and Microsoft Excel.
• Understanding of GCP, clinical study documentation, data quality, and patient confidentiality requirements.
• Ability to identify data discrepancies, maintain accurate records, and communicate effectively with research teams.
• Strong organizational, analytical, time management, and attention-to-detail skills.