Clinical Trial Site Relationship Coordinator
Pubblicato il 17-09-2026 - Medpace in Monza
Overview
In this role you support and expand a network of clinical sites in Europe, focusing on feasibility, site selection, and study start-up. You will partner with cross-functional teams to optimize site performance and intelligence, driving efficient feasibility processes and strong site relationships. The role combines overseeing site relationships, coordinating feasibility activities, and contributing to process improvements across studies. You will work in a fast-paced, mission-driven environment that values collaboration and impact.
Retribuzione / 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
Responsabilità
Provide ongoing site support and identify future business opportunities and feasibility assessments
Develop plans for site contact, follow-up, and relationship management within assigned country
Support management in expediting feasibility, site selection and study start-up
Serve as site relations and excellence partner, maintaining relationships with preferred site networks and flagship sites
Conduct feasibility activities (standalone, blinded, initial, ongoing) and assist with site alignment to studies and therapeutic areas
Research site landscape and intelligence (KOL presence, site capabilities,
country practice standards) relevant to patient population and recruitment
Maintain relationships with network directors, facilitate master CDAs and organize network meetings
Perform regular site performance reviews to ensure quality delivery and address issues
Act as escalation point for site-related issues throughout the study lifecycle
Support process improvement initiatives for feasibility activities and site performance
Serve as main contact for project teams regarding site performance updates and information
Possibly assist with site qualifications visits, audits preparation, and related tasks
May be assigned additional projects and responsibilities as needed
Requisiti fondamentali
Bachelor of Science in health-related field
Minimum 1 year of site and clinical trials experience
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
Strong organizational and prioritization skills
Excellent oral and written communication
Proficient in Microsoft Office applications
Strong communication skills
Organizational and prioritization abilities
Relationship-building and interpersonal aptitude
Microsoft Office applications
GCP knowledge (preferred)
Clinical trials operations familiarity