Clinical Trial Project Manager
Medpace, Inc.
Job SummaryMedpace is seeking an office-based Clinical Project Coordinator to join our Clinical Pharmacology Unit (CPU), to support the development of new medicines and therapies. In this role, you will work directly with our CPU staff to ensure timely management of study activities across early phase studies over a spectrum of diseases. ResponsibilitiesResponsible for managing one or more projects according to Sponsor specifications;Coordinate project start-up, maintenance, and close-out activities;Track study status including patient status, case report form status, safety issues, timelines, etc.;Serve as primary contact for all protocol interpretations and logistical project-related issues; andProvide oversight for staff conducting study-related responsibilities/procedures.QualificationsBachelor’s Degree and 1-3 year of research-related experience; andBroad knowledge of medical terminology and clinical research methodology.Medpace OverviewMedpace is a full-service clinical contract research organization (CRO) providing phase l-lV 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 the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries.Why Medpace?When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.Purpose-Driven WorkWork alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellenceCollaborative CultureContribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust.Leadership throughout Medpace is both accessible and approachableContinuous Growth & DevelopmentOffice based environment with on-site mentorsDefined career paths with clear advancement opportunitiesIndustry renowned onboarding and training programs designed to accelerate professional developmentOngoing training and continuous learning opportunities throughout your careerAn environment that encourages employees to influence change, contribute ideas, and grow quicklyOther Employee BenefitsCompetitive compensation programs that recognize and reward performanceComprehensive health, wellness, retirement, and PTO benefitsOffice based culture with occasional WFH that provides flexibility for eligible positions after trainingCompany-sponsored social events and intramural sportsCincinnati Headquarters ExperienceA modern corporate campus designed to support collaboration and productivityMultiple on-site dining options in the heart of Madison SquareFree on-site parkingConvenient access to on-site 24-7 fitness and wellness facilitiesWhat to Expect NextA Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted.Job SummaryCategory: Clinical Pharmacology & Nursing
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$56.78k - $62.15k
...may vary based on FTE status. Join Our Clinical Research Coordinator Talent Community Cincinnati... ...and enrollment, conduct study visits, manage regulatory documentation, collect and... ...Participant recruitment and enrollment Clinical trials or observational research Regulatory...Full timeWork experience placementWork at officeShift workWeekend work- Cincinnati Children's is seeking Clinical Research Coordinators to support innovative clinical and translational research programs across... ...participant recruitment and enrollment, conduct study visits, manage regulatory documentation, collect and process specimens,...
$61.4k - $78.29k
...Responsibilities Study Conduct/ Clinical Research Practice - Serve as... ...of conducting a clinical trial for complex and multi-center... ...Develop & implement associated projects related to studies under the... ...and report out to PI and or management. Data Management - Oversee data...Full timeLocal areaShift work- Ctifacts is seeking a Clinical Research Coordinator for our Cincinnati, OH site. The role encompasses coordinating Phase I-IV studies following GCPs, SOPs, and regulatory standards. You will manage study visits, consent, data collection, and drug accountability while maintaining...
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$24.46 - $27.73 per hour
...JOB RESPONSIBILITIES Study Conduct/ Clinical Research Practice - Assist in coordinating... ...involved in the clinical research project work. Assist other staff members and coordinators... ..., study coordinators, clinical team, managers and other institutions. Maintain...Full timeWork experience placementLocal areaShift workWeekend work- Velocity Clinical Research, Inc. is seeking a Clinical Research Coordinator I in Cincinnati to manage and coordinate clinical trials per protocol and regulatory standards. You will conduct visits, collect regulatory documents, and ensure timely data entry and safety reporting...
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- ...Sciences, aiming to transition into the Clinical Trials Industry within areas like... ...pathway to an Associate Clinical Trial Manager role in our global Clinical Operations... ...on analytical and academic skills applied to clinical project #J-18808-Ljbffr MedpaceFull timeWork at office
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- ...Coordinator, who will be a member of our global clinical operations team. By working cross... ...enrollment planning for global clinical trials. If you are an individual with a... ...to detail;Ability to prioritize multiple projects and tasks within tight timelines; andExcellent...Contract workWork from home
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