Clinical Trial Site Relationship Coordinator (German Speaking)

Overview

In this role, you will support and strengthen site partnerships across the UK and Hungary to enable efficient feasibility and study start-up. You’ll work closely with the Clinical Operations team to identify new business opportunities, manage site networks, and drive improvements in feasibility processes. You’ll be a key point of contact for sites, ensuring high-quality study delivery and rapid resolution of issues. This position offers growth within a globally respected CRO and the chance to shape how we engage sites and feasibility strategies.

Pay / Benefits

• Flexible work environment
• Competitive compensation and benefits package
• Competitive PTO packages
• Structured career paths with opportunities for professional growth
• Company-sponsored employee appreciation events
• Employee health and wellness initiatives

Responsibilities

• Support ongoing site relationships and explore future business opportunities with feasibility assessments
• Develop plans for site contact, follow-up, and performance reviews
• Assist management with expedited feasibility, site selection, and study start-up
• Serve as site relations partner to maintain and expand network sites within country
• Conduct regular feasibility activities and align site capabilities with studies and therapeutic areas
• Build and maintain an intelligence database on sites and country considerations
• Lead process improvement initiatives for feasibility activities
• Act as main contact for project teams on site performance issues and updates
• Coordinate site qualifications visits and support for site audits as needed

Key requirements

• Bachelor of Science in health-related field
• Minimum 1 year of site and clinical trials experience (more for senior roles)
• CRA experience is an asset
• Knowledge of drug development, clinical trial management and GCP preferred
• Knowledge of medical terminology and clinical patient management preferred
• Fluency in English; German is a plus
• Strong organizational and prioritization skills
• Excellent oral and written communication skills
• Proficient in Microsoft Office applications

• organizational skills
• prioritization
• excellent communication
• knowledge of GCP and clinical trial management
• Microsoft Office proficiency
• site management and feasibility competencies

…