Clinical Trial Project Manager - Cardiovascular, Renal, Metabolic(Sign-On Bonus Eligible)Job Locations

　　United States-OH-Cincinnati | United States | United States-TX-Irving(Dallas) | United States-CO-Denver

　　CategoryClinical Trial ManagementJob Summary

　　Medpace is the leading CRO for Biotech companies and is continuing to addestablished Clinical Trial Managers and Project Managers with a focus onCardiovascular, Renal, and Metabolic therapeutic areas to join ourClinical Trial Management Group. We have just expanded our campus inCincinnati and have offices in Dallas and Denver and provide remoteflexibility with relevant experience. We offer a very competitivesalary/bonus program, plus equity grants which have become very lucrativefor our associates.

　　Responsibilities

　　Manage and provide accountability for day-to-day operations of the project,as defined by the contract and according to ICH/GCP and all other applicablelaws, rules, and regulationsServe as primary Sponsor contact for operational project-specific issues andstudy deliverablesMaintain in depth knowledge of protocol, therapeutic area, and indicationProvide cross-functional oversight of internal project team members anddeliverables, which includes ensuring all necessary project-specifictraining 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 ClinicalResearch Associates and monitoring deliverablesQualifications

　　Bachelor's degree in a health-related field; Advanced degree in ahealth-related field preferredExperience in Phases 1-4; Phases 2-3 preferred5+ years as a project/clinical trial manager within a CRO; required forhome-basedManagement of overall project timelineStrong leadership skills

　　Medpace Overview

　　Medpace 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 theglobal development of safe and effective medical therapeutics through itsscientific and disciplined approach. We leverage local regulatory andtherapeutic 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 thelives of countless patients and families who face hundreds of diseases acrossall key therapeutic areas. The work we do today will improve the lives ofpeople living with illness and disease in the future.Cincinnati PerksCincinnati Campus OverviewHybrid work-from-home options (dependent upon position and level)Competitive PTO packages, starting at 20+ daysFlexible work hoursDiscounted tuition for UC online programsCompany-sponsored employee appreciation eventsEmployee health and wellness initiativesCommunity involvement with local nonprofit organizationsCompetitive compensation and benefits packageStructured career paths with opportunities for professional growthPartnership and discount with onsite childcareDiscounts on local sports games, local fitness gyms and attractionsOfficial Sponsor of FC CincinnatiModern, ecofriendly campus with an on-site fitness center, bar, andrestaurants

　　AwardsRecognized by Forbes as one of America's Best Mid-size Companies in 2021,2022 and 2023Continually recognized with CRO Leadership Awards from Life Science Leadermagazine based on expertise, quality, capabilities, eliability, andcompatibility

　　What to Expect NextA Medpace team member will review your qualifications and, if interested,you will be contacted with details for next steps.

　　EO/AA Employer M/F/Disability/Vets