QC Data Coordinator (Clinical Research) - 247570 This range is provided by Medix™. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more. Base pay range $45,000.00/yr - $65,000.00/yr Direct message the job poster from Medix™ The Clinical Research QC Data Specialist is responsible for reviewing and validating clinical trial data captured in Electronic Data Capture (EDC) systems to ensure accuracy, consistency, and regulatory compliance. This position supports overall data quality by identifying errors, reconciling discrepancies, and working closely with clinical teams to maintain reliable datasets for study reporting and analysis. The role requires strong technical aptitude, attention to detail, and the ability to navigate complex data workflows within clinical research environments. Core Responsibilities Data Review & Validation: Evaluate clinical data for completeness and accuracy, flag issues, and initiate queries as needed. EDC System Oversight: Use EDC platforms to input, verify, and reconcile study data throughout various phases of the trial. Issue Resolution: Partner with CRAs, coordinators, and site personnel to clarify questionable data and correct inconsistencies. Quality Checks: Conduct routine quality control reviews to ensure databases meet study standards prior to analysis. Documentation Support: Contribute to the creation and maintenance of study documentation, including data review guidelines and validation procedures. Regulatory Compliance: Follow study protocols, SOPs, and regulatory standards such as ICH‑GCP when handling and reviewing data. System Testing: Participate in user testing for updates or new releases of EDC systems and data management tools to ensure functionality aligns with study needs. Key Skills & Qualifications Technical Proficiency: Hands‑on experience with EDC systems; familiarity with data analysis tools is beneficial. Analytical Ability: Strong problem‑solving skills with the ability to identify trends, errors, and data quality issues. Detail Orientation: Careful and methodical approach to data review and protocol adherence. Communication Skills: Able to effectively collaborate with cross‑functional teams, including data managers, site staff, and statisticians. Regulatory Understanding: Solid knowledge of clinical research guidelines and industry standards, especially ICH‑GCP. Seniority level: Entry level Employment type: Full-time Job function: Administrative, Quality Assurance, and Research Benefits Medical insurance Vision insurance 401(k) Referrals increase your chances of interviewing at Medix™ by 2x #J-18808-Ljbffr Medix™
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