Clinical Data Quality Specialist - Onsite in Doral

Suncoast Research Associates, LLC; Florida; On-site; USD 55,000 - 70,000; Full time

Benefits offered by this job

Health insurance

Dental insurance

Vision insurance

Life insurance

Paid time off

Job summary

Suncoast Research Associates, LLC in Doral, Florida, seeks a Quality Control Specialist to ensure the accuracy and integrity of clinical data across multiple studies. You will uphold regulatory standards and support sponsor timelines while contributing to a trusted, inspection-ready research environment.

Key responsibilities include QC review across therapeutic areas, protocol interpretation, and cross-functional collaboration to resolve data queries.

Qualifications

• Strong attention to detail with a consistent commitment to accuracy.
• Excellent organizational skills and the ability to manage competing priorities under deadline.
• Strong written and verbal communication skills.
• Proficiency in Excel and the Microsoft Office suite.
• Previous experience in quality assurance or a related clinical research role is preferred.

Responsibilities

• Perform accurate and timely quality control review of clinical data across studies and therapeutic areas.
• Review and interpret protocols, amendments, and study manuals; verify source documents for protocol compliance.
• Identify, document, and escalate data quality issues as needed.
• Support monitoring visits, audits, and inspections with audit-ready QC documentation.
• Collaborate cross-functionally with coordinators, investigators, monitors, sponsors, CROs, and vendors to resolve data queries.

Skills

Attention to detail

Organizational skills

Communication skills

Excel

Clinical data QA

GCP knowledge

Tools

EDC systems

Microsoft Office

Job description

Suncoast Research Associates, LLC in Doral, Florida, seeks a Quality Control Specialist to ensure the accuracy and integrity of clinical data across multiple studies. You will uphold regulatory standards and support sponsor timelines while contributing to a trusted, inspection-ready research environment.

Key responsibilities include QC review across therapeutic areas, protocol interpretation, and cross-functional collaboration to resolve data queries.