Clinical Research Associate (CRA) responsible for site performance and compliance in a specified country, managing all phases of clinical trial conduct at assigned sites.
ensure adherence to ICH-GCP, local regulations, and company policies, while fostering strong site relationships and expanding the research territory.
conduct remote and on-site monitoring, oversee regulatory documentation, participate in site selection, handle issue resolution, and support audits; collaborate with cross-functional teams including regulatory, pharmacovigilance, and legal; contribute as subject matter expert and mentor within the CRA team.
Associate's degree or bachelor’s with 5+ years in healthcare/clinical research, including 2+ years of site management experience in biopharma or CRO; proficiency in GCP, clinical trial processes, and data management; fluent in local language and English; valid driver's license preferred.
global trial oversight, site management, 65-75% travel (~2-3 days/week), remote work, experience across phases of clinical trials, strong understanding of GCP/ICH, and regulatory compliance in diverse therapy areas.
remote with extensive domestic and international travel.
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