Senior Clinical Trial Project Manager – Chile (Bío Bío)

OverviewOur activities in South America are expanding! Medpace is the leading CRO for Biotech companies and we are seeking to add an established Clinical Trial Manager to join our Clinical Trial Management Group in Chile. Our therapeutic areas of focus include Oncology / Hematology, Cardiovascular / Metabolic, Infectious Disease, Neuroscience, and more. We offer a very competitive salary / bonus programs along with local benefits.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, which includes 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 executionManage study vendors where applicableManage site quality and monitoring deliverablesQualificationsBachelor's degree in a health-related field; Advanced degree in a health-related field preferredExperience in Phases 1-4; Phases 2-3 preferred5+ years as a project / clinical trial manager within a CRO requiredManagement 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 general 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.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 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.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

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• Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibilityWhat to Expect NextA Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.Bachelor's degree in a health-related field; Advanced degree in a health-related field preferredExperience in Phases 1-4; Phases 2-3 preferred5+ years as a project / clinical trial manager within a CRO requiredManagement of overall project timelineBid defense experience preferredStrong leadership skills #J-
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