13 set - Milano
Medpace
ppOur 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. /p pIf 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. /p h3Responsibilities /h3 ul liProvide ongoing support of sites, including identifying and discussing future new business opportunities and feasibility assessments; /li liDevelop effective plans for site contact and follow-up; /li liSupport management in expediting feasibility, site selection and study start-up; and /li liMay be responsible for other projects and responsibilities as assigned. /li liServe as site relations and excellence partner by providing oversight and building/retaining relationships of assigned sites within assigned country; /li liConducting/expediting feasibility activities (standalone, blinded, initial, ongoing), supporting Management with site selection/alignment with studies and/or therapeutic areas, and study start-up; /li liProactively 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; /li liBuilding and maintaining relationships with preferred site networks/flagship sites which includes facilitating master CDAs and holding meetings with network directors /li liConducting regular performance reviews for sites participating to our studies, ensuring quality study delivery /li liServe as an escalation point for site related issues throughout the life cycle of a study /li liProvide ongoing support of sites,
including identifying and discussing future new business; /li liDevelop effective plans for site contacts, troubleshooting, and follow-up; /li liDevelop an intelligence database with site and country intelligence /li liSupport Management with process improvement initiatives regarding feasibility activities /li liServe as main point of contact for project teams regarding site performance issues and updates on pertinent site information; and /li liMay be responsible for other projects and responsibilities as assigned, including site Qualification Visits, prepping/consultation support for site audits, etc. /li /ul h3Qualifications /h3 ul liMinimum a Bachelor of Science in health-related field; /li liMinimum 1 years' site and clinical trials experience (more experience for the more senior positions required); /li liCRA experience is an asset; /li liKnowledge of drug development, clinical trial management and operational procedures, including GCP guidelines preferred; /li liKnowledge of medical terminology and clinical patient management preferred; /li liFluency in English; /li liDemonstrated organizational and prioritization skills; /li liExcellent oral and written communication skills; and /li liProficient knowledge of Microsoft Office applications. /li /ul h3WHY MEDPACE? /h3 pAt 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. /p h3Compensation /h3 pEUR €40,000.00/Yr. - EUR €58,000.00/Yr. /p h3Medpace Overview /h3 pMedpace 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. /p h3Why Medpace? /h3 pWhen you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration. /p h3Purpose-Driven Work /h3 ul liWork alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence /li /ul h3Collaborative Culture /h3 ul liContribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust. /li liLeadership throughout Medpace is both accessible and approachable /li /ul h3Continuous Growth Development /h3 ul liOffice based environment with on-site mentors /li liDefined career paths with clear advancement opportunities /li liIndustry renowned onboarding and training programs designed to accelerate professional development /li liOngoing training and continuous learning opportunities throughout your career /li liAn environment that encourages employees to influence change, contribute ideas, and grow quickly /li /ul h3Other Employee Benefits /h3 ul liCompetitive compensation programs that recognize and reward performance /li liComprehensive health, wellness, retirement, and PTO benefits /li liOffice based culture with occasional WFH that provides flexibility for eligible positions after training /li liCompany-sponsored social events /li /ul pPlease note benefits may vary based on country. /p /p #J-18808-Ljbffr
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