Medpace is the leading CRO for Biotech companies andis continuing to add Clinical Trial Managers of differentexperience levels to join our Clinical Trial Management Group inLondon. Clinical Trial Managers with expertise in Oncology arewelcome to continue to work in their area of expertise or to expandto a new therapeutic area . We provide remote flexibility only withrelevant experience. We offer a very competitive salary/bonusprogram, plus equity grants which have become very lucrative forour associates. Responsibilities Manage and provide accountabilityfor day-to-day operations of the project, as defined by thecontract and according to ICH/GCP and all other applicable laws,rules, and regulations Serve as primary Sponsor contact foroperational project-specific issues and study deliverables Maintainin depth knowledge of protocol, therapeutic area, and indicationProvide cross-functional oversight of internal project team membersand deliverables, which includes ensuring all necessaryproject-specific training is provided Review and provide input forstudy protocol, edit check specifications, data analysis plan, andfinal study report, when applicable Develop operational projectplans Manage risk assessment and execution Responsible formanagement of study vendor Manage site quality, including directsupervision of project Clinical Research Associates and monitoringdeliverables Qualifications Bachelor’s degree in a health or lifescience-related field; Advanced degree in a health or lifescience-related field preferred; Experience in Phases 1-4; Phases2-3 preferred; Minimum of 5 years of Clinical Trial Managementexperience, CRO experience preferred; 5+ years of ProjectManager/Clinical Trial Manager experience at a CRO required for aremote-based role; Management of overall project timeline; Biddefense experience preferred; and Strong leadership skills. MedpaceOverviewMedpace is a full-service clinical contract researchorganization (CRO). We provide Phase I-IV clinical developmentservices to the biotechnology, pharmaceutical and medical deviceindustries. Our mission is to accelerate the global development ofsafe and effective medical therapeutics through its scientific anddisciplined approach. We leverage local regulatory and therapeuticexpertise 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. WhyMedpace?People. Purpose. Passion. Make a Difference Tomorrow. JoinUs Today. The work we’ve done over the past 30+ years haspositively impacted the lives of countless patients and familieswho face hundreds of diseases across all key therapeutic areas. Thework we do today will improve the lives of people living withillness and disease in the future. Medpace Perks Flexible workenvironment Competitive compensation and benefits packageCompetitive PTO packages Structured career paths with opportunitiesfor professional growth Company-sponsored employee appreciationevents Employee health and wellness initiatives Awards Recognizedby Forbes as one of Americas Most Successful Midsize Companies in2021, 2022, 2023 and 2024 Continually recognized with CROLeadership Awards from Life Science Leader magazine based onexpertise, quality, capabilities, reliability, and compatibilityWhat to Expect Next A Medpace team member will review yourqualifications and, if interested, you will be contacted withdetails for next steps. EO/AA EmployerM/F/Disability/Vets
