Description
Celerion is hiring a Clinical Research Data Manager to manage data workflows through quality control and data entry, maintain study timelines, ensure regulatory compliance, and coordinate with sponsors, sites, and internal departments. The role includes supervising and training staff, developing QC and data-entry SOPs, presenting processes to sponsors and auditors, leading process-improvement and problem-solving initiatives, and participating in audits and inspections. A bachelor’s degree in a related field and 1–2 years of supervisory or trainer/leader experience are required; clinical data experience and knowledge of GCP, ICH, and 21 CFR Part 11 are preferred.
