Clinical Trial Site Relationship Coordinator
OverviewIn 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 environmentCompetitive compensation and benefits packageCompetitive PTO packagesStructured career paths with opportunities for professional growthCompany-sponsored employee appreciation eventsEmployee health and wellness initiatives
Responsabilità
Provide ongoing site support and identify future business opportunities and feasibility assessmentsDevelop plans for site contact, follow-up, and relationship management within assigned countrySupport management in expediting feasibility, site selection and study start-upServe as site relations and excellence partner, maintaining relationships with preferred site networks and flagship sitesConduct feasibility activities (standalone, blinded, initial, ongoing) and assist with site alignment to studies and therapeutic areasResearch site landscape and intelligence (KOL presence, site capabilities,
country practice standards) relevant to patient population and recruitmentMaintain relationships with network directors, facilitate master CDAs and organize network meetingsPerform regular site performance reviews to ensure quality delivery and address issuesAct as escalation point for site-related issues throughout the study lifecycleSupport process improvement initiatives for feasibility activities and site performanceServe as main contact for project teams regarding site performance updates and informationPossibly assist with site qualifications visits, audits preparation, and related tasksMay be assigned additional projects and responsibilities as needed
Requisiti fondamentali
Bachelor of Science in health-related fieldMinimum 1 year of site and clinical trials experienceCRA experience is an assetKnowledge of drug development, clinical trial management and GCP preferredKnowledge of medical terminology and clinical patient management preferredFluency in EnglishStrong organizational and prioritization skillsExcellent oral and written communicationProficient in Microsoft Office applicationsStrong communication skillsOrganizational and prioritization abilitiesRelationship-building and interpersonal aptitudeMicrosoft Office applicationsGCP knowledge (preferred)Clinical trials operations familiarity
Retribuzione / Benefits
Flexible work environmentCompetitive compensation and benefits packageCompetitive PTO packagesStructured career paths with opportunities for professional growthCompany-sponsored employee appreciation eventsEmployee health and wellness initiatives
Responsabilità
Provide ongoing site support and identify future business opportunities and feasibility assessmentsDevelop plans for site contact, follow-up, and relationship management within assigned countrySupport management in expediting feasibility, site selection and study start-upServe as site relations and excellence partner, maintaining relationships with preferred site networks and flagship sitesConduct feasibility activities (standalone, blinded, initial, ongoing) and assist with site alignment to studies and therapeutic areasResearch site landscape and intelligence (KOL presence, site capabilities,
country practice standards) relevant to patient population and recruitmentMaintain relationships with network directors, facilitate master CDAs and organize network meetingsPerform regular site performance reviews to ensure quality delivery and address issuesAct as escalation point for site-related issues throughout the study lifecycleSupport process improvement initiatives for feasibility activities and site performanceServe as main contact for project teams regarding site performance updates and informationPossibly assist with site qualifications visits, audits preparation, and related tasksMay be assigned additional projects and responsibilities as needed
Requisiti fondamentali
Bachelor of Science in health-related fieldMinimum 1 year of site and clinical trials experienceCRA experience is an assetKnowledge of drug development, clinical trial management and GCP preferredKnowledge of medical terminology and clinical patient management preferredFluency in EnglishStrong organizational and prioritization skillsExcellent oral and written communicationProficient in Microsoft Office applicationsStrong communication skillsOrganizational and prioritization abilitiesRelationship-building and interpersonal aptitudeMicrosoft Office applicationsGCP knowledge (preferred)Clinical trials operations familiarity