CRA - FSP - Central Poland
Core
Conduct remote and on-site clinical monitoring to ensure protocol and regulatory compliance, manage site processes, and guarantee data reliability for pharmaceutical clinical trials.
Role type
Level II Clinical Research Associate (CRA)
Builds
Clinical trials for pharmaceutical and biotech sponsors
Domain
Clinical Research / Pharmaceuticals
Deliverable
client delivery
Required skills
risk-based monitoring, root cause analysis, critical thinking, problem-solving, data accuracy verification (SDR, SDV, CRF review), physical inventory management, regulatory compliance knowledge (ICH-GCP), audit readiness, site initiation, trial close-out
Preferred skills
business writing, collaborative relationship building
Technologies
None explicitly stated
Responsibilities
Monitor investigator sites using a risk-based approach to identify failures and implement corrective actions; ensure data accuracy through source data review and case report form verification; manage investigator payments and initiate new clinical trial sites; perform trial close-out and retrieval of materials; ensure essential trial documents are complete and compliant.
Seniority
Mid-level IC