Senior Clinical Research Associate

Experteer Overview

In this role you will oversee clinical trial monitoring to ensure compliance with protocols, regulatory standards and GCP. You will lead site visits, assess performance, and support investigators to drive successful trial execution. You will collaborate with cross-functional teams to ensure timely data collection and reporting, and you will train and mentor site staff to uphold high conduct standards. This position offers the opportunity to influence trial quality at scale within a mission-driven, inclusive environment. You will work closely with sites and stakeholders to enable efficient, compliant studies and impactful outcomes.

Retribuzione / Benefits

• Monitor trial sites for adherence to study protocols, regulatory requirements, and GCP.
• Conduct site visits to assess performance, resolve issues, and support trial execution.
• Collaborate with cross-functional teams to ensure timely and accurate data collection and reporting.
• Provide training and guidance to site staff and other CRAs to maintain high standards.
• Build and maintain relationships with site personnel and stakeholders to facilitate smooth operations.

Responsabilità

• Bachelor in a relevant scientific discipline or healthcare-related field.
• Extensive experience as a Clinical Research Associate with strong understanding of trial processes and regulatory requirements.
• Ability to manage multiple sites and projects with strong organizational and problem-solving skills.
• Expertise in monitoring practices, data integrity, and site management with proficiency in clinical trial software and tools.
• Excellent communication, interpersonal, and stakeholder management skills with influencing and compliance capabilities.
• Willingness to travel approximately 60%.

Requisiti fondamentali

• annual leave entitlements
• health insurance offerings
• retirement planning
• LifeWorks Global EAP
• Life assurance
• flexible country-specific optional benefits