OverviewMedpace Stirling, Scotland, United Kingdom is seeking a Clinical Trial Manager (Associate Director) to join the Clinical Trial Management Group in Stirling. Medpace is a leading CRO for biotech companies, and the role supports oncology and other therapy areas. Remote flexibility is offered only with relevant experience. We provide a competitive salary/bonus program, plus equity grants. ResponsibilitiesManage 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 regulationsServe as primary Sponsor contact for operational project-specific issues and study deliverablesMaintain in-depth knowledge of protocol, therapeutic area, and indicationProvide cross-functional oversight of internal project team members and deliverables, including ensuring all necessary project-specific training is providedReview and provide input for study protocol, edit check specifications, data analysis plan, and final study report, when applicableDevelop operational project plansManage risk assessment and executionResponsible for management of study vendorManage site quality, including direct supervision of project Clinical Research Associates and monitoring deliverablesQualificationsBachelor’s degree in a health or life science-related field; Advanced degree preferredExperience in Phases 1-4; Phases 2-3 preferredMinimum of 5 years of Clinical Trial Management experience, CRO experience preferred5+ years of Project Manager/Clinical Trial Manager experience at a CRO required for a remote-based roleManagement of overall project timelineBid defense experience preferredStrong leadership skillsMedpace OverviewMedpace 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 a scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across 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.Why Medpace?People. 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 diseases across key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.Medpace PerksFlexible work environmentCompetitive compensation and benefits packageCompetitive PTO packagesStructured career paths with opportunities for professional growthCompany-sponsored employee appreciation eventsEmployee health and wellness initiativesAwardsRecognized by Forbes as one of America\'s Most Successful Midsize Companies in 2021, 2022, 2023 and 2024Continually recognized with CRO Leadership Awards from Life Science Leader magazineWhat To Expect NextA Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.Seniority levelNot ApplicableEmployment typeFull-timeJob functionResearch, Analyst, and Information TechnologyIndustriesPharmaceutical ManufacturingReferrals increase your chances of interviewing at Medpace by 2x #J-18808-Ljbffr