Senior Clinical Research Associate

📋 Description Oversee clinical monitoring activities ensuring protocols, regulatory requirements, and quality Perform and coordinate monitoring per ICH-GCP and SOPs. Conduct site visits (pre-study, initiation, interim, close-out) with protocol compliance and Act as primary contact for assigned sites, building relationships with investigators and teams. Provide protocol training and guidance to sites and project teams. Monitor site performance indicators (enrollment, data quality, deviations, issues). 🎯 Requirements Bachelor’s degree in a relevant scientific discipline or equivalent. Minimum 3 years in clinical operations with at least 2 years in clinical monitoring. Experience in pharmaceutical/biotech trials; oncology/hematology experience desirable. Strong knowledge of clinical trial processes, ICH-GCP, and regulatory requirements. Experience managing sites and ensuring protocol/regulatory compliance. Excellent written and verbal communication; fluent English required. 🎁 Benefits Opportunity to work on innovative clinical programs with global impact. Remote work flexibility. Exposure to international operations and multidisciplinary teams. Professional growth within a science-focused environment. Continuous learning and development initiatives. Chance to contribute to healthcare advancements and patient outcomes.