Clinical Trial Site Relationship Coordinator (German Speaking)
Core
Full-time Clinical Trial Site Relationship Coordinator supporting pre-award and post-award study feasibilities, building strategic relationships with clinical sites, and developing strategies for conducting feasibilities in the UK and Hungary.
Role type
Clinical Trial Site Relationship Coordinator
Builds
Feasibility assessments, site selection, and study start-up plans for clinical trials
Domain
Clinical Research / Contract Research Organization (CRO)
Deliverable
client delivery
Required skills
Clinical research experience, site relationship management, feasibility assessment, site selection, study start-up support, site performance review, intelligence database development, process improvement, site qualification visit support, audit preparation
Preferred skills
CRA experience, knowledge of drug development, clinical trial management, GCP guidelines, medical terminology, clinical patient management
Technologies
Microsoft Office
Responsibilities
Provide ongoing support of sites including identifying and discussing future new business opportunities and feasibility assessments; Develop effective plans for site contact and follow-up; Support management in expediting feasibility, site selection and study start-up; Serve as site relations and excellence partner by providing oversight and building/retaining relationships of assigned sites within assigned country; Conducting/expediting feasibility activities (standalone, blinded, initial, ongoing), supporting Management with site selection/alignment with studies and/or therapeutic areas, and study start-up; Proactively research and understand specified site landscape/intelligence (KOL presence and knowledge, site capabilities, country standard of care and medical practices, etc.) as it relates to specific patient population, recruitment, and retention; Building and maintaining relationships with preferred site networks/flagship sites which includes facilitating master CDAs and holding meetings with network directors; Conducting regular performance reviews for sites participating to our studies, ensuring quality study delivery; Serve as an escalation point for site related issues throughout the life cycle of a study; Develop an intelligence database with site and country intelligence; Support Management with process improvement initiatives regarding feasibility activities; Serve as main point of contact for project teams regarding site performance issues and updates on pertinent site information; May be responsible for other projects and responsibilities as assigned, including site Qualification Visits, prepping/consultation support for site audits, etc.
Seniority
Entry-level to Mid-level (1+ years experience required)
