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.