Clinical Trial QA & Data Entry Specialist

Tribe Clinical Research; Greenville (SC); On-site; USD 55,000 - 75,000; Full time

Job summary

Tribe Clinical Research in Greenville, SC seeks a QA Specialist to enter clinical trial data, follow GCP/ICH, identify errors, and maintain timelines. The role requires strong computer skills and an outgoing, client-facing demeanor to support site personnel and sponsors.

You will enter data into Clinical Conductor, perform QA checks on source documents, coordinate investigator signatures, and assist monitors during visits.

Qualifications

• Accurate data entry with knowledge of GCP/ICH guidelines.
• Strong time management and communication skills.
• Experience collaborating with study personnel and sponsors.

Responsibilities

• Timely data entry and query resolution.
• Collaboration with site personnel and sponsors.
• Directs investigator signature process.
• Greets monitors and reviews source documents.

Skills

Time management

Computer proficiency

Customer Service

Tools

Clinical Conductor

Job description

Tribe Clinical Research in Greenville, SC seeks a QA Specialist to enter clinical trial data, follow GCP/ICH, identify errors, and maintain timelines. The role requires strong computer skills and an outgoing, client-facing demeanor to support site personnel and sponsors.

You will enter data into Clinical Conductor, perform QA checks on source documents, coordinate investigator signatures, and assist monitors during visits.