Clinical Trial Manager - Italy - Neuroscience / Ophthalmology

ph3Job Overview /h3 pMedpace is the leading CRO for Biotech companies and is continuing to add Clinical Trial Managers of different experience levels to join our Clinical Trial Management Group in Italy, particularly in our Milan office. Clinical Trial Managers with expertise in Neuroscience and CNS are welcome to continue to work in their area of expertise or to expand to a new therapeutic area. We provide remote flexibility only with relevant experience (after probation). We offer a very competitive salary/bonus program, plus equity grants which have become very lucrative for our associates. /p h3Responsibilities /h3 ul liManage and provide accountability for day-to-day operations of the project, as defined by the contract and according to ICH/GCP and all other applicable laws, rules, and regulations /li liServe as primary Sponsor contact for operational project-specific issues and study deliverables /li liMaintain in depth knowledge of protocol, therapeutic area, and indication /li liProvide cross-functional oversight of internal project team members and deliverables, which includes ensuring all necessary project-specific training is provided /li liReview and provide input for study protocol, edit check specifications, data analysis plan, and final study report, when applicable /li liDevelop operational project plans /li liManage risk assessment and execution /li liResponsible for management of study vendor /li liManage site quality, including direct supervision of project Clinical Research Associates and monitoring deliverables /li /ul h3Qualifications /h3 ul liBachelor’s degree in a health or life science-related field; Advanced degree in a health or life science-related field preferred /li liExperience in Phases 1-4; Phases 2-3 preferred /li liMinimum of 2 years of Clinical Trial Management experience, CRO experience preferred /li liManagement of overall project timeline /li liBid defense experience preferred, and /li liStrong leadership skills /li /ul h3Medpace Overview /h3 pMedpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV 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 its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries. /p h3Why Medpace? /h3 pPeople. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future. /p h3Medpace Perks /h3 ul liFlexible work environment /li liCompetitive compensation and benefits package /li liCompetitive PTO packages /li liStructured career paths with opportunities for professional growth /li liCompany-sponsored employee appreciation events /li liEmployee health and wellness initiatives /li /ul h3Awards /h3 ul liRecognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024 /li liContinually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility /li /ul h3What To Expect Next /h3 pA Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps. /p /p #J-18808-Ljbffr