Clinical Trial Site Relationship Coordinator

ph3Job Summary /h3pOur clinical activities are growing rapidly, and we are currently seeking a full-time Clinical Trial Site Relationship Coordinator to join our vibrant Clinical Operations team in Italy, Milan. This is a fantastic opportunity to work on pre-award and post-award study feasibilities, build and maintain strategic relationships with our network of sites, and develop key strategies to effectively conduct feasibilities across Europe. This position will fit someone who has previous clinical research experience or perhaps a CRA who would like to reduce travel. If you want an exciting career within a company that excels in delivering innovative research and development of cutting edge drugs, where you can grow your potential, then this is the opportunity for you. /ph3Category: Clinical Trial Management /h3h3Clinical Trial Site Relationship Coordinator • milan, lombardy, Italy /h3h3Responsibilities /h3ulliProvide ongoing support of sites, including identifying and discussing future new business opportunities and feasibility assessments; /liliDevelop effective plans for site contact and follow-up; /liliSupport management in expediting feasibility, site selection and study start-up; /liliandMay be responsible for other projects and responsibilities as assigned. /liliServe as site relations and excellence partner by providing oversight and building/retaining relationships of assigned sites within assigned country; /liliConducting/expediting feasibility activities (standalone, blinded, initial, ongoing), supporting Management with site selection/alignment with studies and/or therapeutic areas, and study start-up; /liliProactively 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; /liliBuilding and maintaining relationships with preferred site networks/flagship sites which includes facilitating master CDAs and holding meetings with network directors; /liliConducting regular performance reviews for sites participating to our studies, ensuring quality study delivery; /liliServe as an escalation point for site related issues throughout the life cycle of a study; /liliProvide ongoing support of sites, including identifying and discussing future new business; /liliDevelop effective plans for site contacts, troubleshooting, and follow-up; /liliDevelop an intelligence database with site and country intelligence; /liliSupport Management with process improvement initiatives regarding feasibility activities; /liliServe as main point of contact for project teams regarding site performance issues and updates on pertinent site information; /liliandMay be responsible for other projects and responsibilities as assigned, including site Qualification Visits, prepping/consultation support for site audits, etc. /li /ulh3Qualifications /h3ulliMinimum a Bachelor of Science in health-related field; /liliMinimum 1 years' site and clinical trials experience (more experience for the more senior positions required); /liliCRA experience is an asset; /liliKnowledge of drug development, clinical trial management and operational procedures, including GCP guidelines preferred; /liliKnowledge of medical terminology and clinical patient management preferred; /liliFluency in English; /liliDemonstrated organizational and prioritization skills; /liliExcellent oral and written communication skills; /liliandProficient knowledge of Microsoft Office applications. /li /ulh3WHY MEDPACE? /h3pAt Medpace, you will find work that is both challenging and rewarding. At Medpace, you will be given the tools and training to succeed. At Medpace, you will be rewarded for strong performance and provided opportunities to grow professionally. /ph3Medpace Overview /h3pMedpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries. /ppOffice based culture with on-site mentorsDefined career paths with clear advancement opportunitiesIndustry renowned onboarding and training programs designed to accelerate professional developmentOngoing training and continuous learning opportunities throughout your careerAn environment that encourages employees to influence change, contribute ideas, and grow quickly /ph3Other Employee Benefits /h3ulliCompetitive compensation programs that recognize and reward performance /liliComprehensive health, wellness, retirement, and PTO benefits /liliOffice based culture with occasional WFH that provides flexibility for eligible positions after training /liliCompany-sponsored social events /li /ulpPlease note benefits may vary based on country. /p /p #J-18808-Ljbffr