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Medpace Inc Clinical Research Project Manager - Denver, CO (Sign-On Bonu in Denver, Colorado

Clinical Research Project Manager - Denver, CO (Sign-On Bonus Eligible)Job LocationsUnited States-CO-DenverCategoryClinical OperationsOverviewMedpace 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 approximately 3,500 people across almost 40 countries.Job SummaryMedpace is the leading CRO for Biotech companies and is continuing to addsenior-level Directors and established Project Managers to join our ClinicalTrial Management Group in Denver, CO. Our therapeutic areas of focus includeOncology, Cardiovascular/Metabolic, Infectious Disease, CNS and more.We have just expanded our campus in Cincinnati and have offices in Dallas andDenver and provide remote flexibility with relevant experience. We offer avery competitive salary/bonus program, plus equity grants which havebecome very lucrative for our associates.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 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 deliverablesQualificationsBachelor'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 timelineBid defense experienceStrong leadership skillsWhy Medpace?When you join Medpace, you become part of a team dedicated to supporting thedevelopment of ground-breaking drugs and devices. Our employees provide hopefor those living with debilitating diseases. We invite you to be a part ofsomething that is impacting millions of people around the globe while enjoyinga competitive total compensation and benefits package and internal growthopportunities.Awards:Medpace historically named a Top Cincinnati Workplace by the CincinnatiEnquirerMedpace ranks amongst top CROs for site ratings across all 10 importantattributes including CRA training, preparation and organization,accessibility of staff, open communication, and ensuring timely drugavailabiliContinually recognized with CRO Leadership Awards from Life Science Leadermagazine based on expertise, quality, capabilities, reliability, andcompatibilityWhat to Expect Next:A member of our recruitment team will review your qualifications and, ifinterested, you will be contacted for an interview.*WARNING:Please beware of phishing scams that offer opportunities withMedpace in exchange for sending money. These scammers pose as legitimateemployees from actual companies. Please be advised that a Medpace employeewill never ask you for a credit card, send you a check, or ask you for anytype of payment as part of consideration for a role with our company. All ofour careers require that you first complete an online application and gothrough some sort of intervie