Senior Clinical Data Coordinator | EDC & QC Lead

ProPharma; Raleigh (NC); On-site; USD 70,000 - 100,000; Full time

Job summary

ProPharma in the United States is seeking a Senior Clinical Data Coordinator (FSP/Contractor) to oversee data management activities for Phase I–III clinical trials, ensuring the data are accurate, timely, and compliant with ICH/GCP guidelines. You will perform data review, UAT of clinical databases, QC routines, and maintain Data Management documentation, contributing to high-quality deliverables and project timelines.

Experience with EDC systems such as Oracle Inform is required or preferred.

Qualifications

• Bachelor's degree or allied health certification required or equivalent experience.
• Minimum 3 years of data management experience.
• Experience with Electronic Data Capture (EDC) systems required.
• Oracle Inform EDC experience preferred.
• Oncology or inflammatory therapeutic area experience preferred.

Responsibilities

• Perform ongoing data review, including reconciliation of data streams and SAE reconciliation with the safety database.
• Perform User Acceptance Testing (UAT) of clinical databases.
• Perform Quality Control (QC) of clinical databases.
• Update Data Management documentation as needed.

Skills

Data management

Quality control

UAT testing

Documentation updates

Education

Bachelor's degree or allied health certification

Tools

Oracle Inform EDC

Job description

ProPharma in the United States is seeking a Senior Clinical Data Coordinator (FSP/Contractor) to oversee data management activities for Phase I–III clinical trials, ensuring the data are accurate, timely, and compliant with ICH/GCP guidelines. You will perform data review, UAT of clinical databases, QC routines, and maintain Data Management documentation, contributing to high-quality deliverables and project timelines.

Experience with EDC systems such as Oracle Inform is required or preferred.