Medpace, an Official Partner of FC Cincinnati, will be hosting the Medpace Career Fair at TQL Stadium on Thursday, September 12th. This event will be highlighting primarily Entry Level opportunities, and targeting candidates with backgrounds in Life Sciences, Biomedical Engineering, Math and Statistics. Prepare your CVs and join us to learn more about the CRO industry, and meet with hiring managers for 10+ positions. The event will be hosted in the Medpace Tunnel Club, with on-site parking, food, and open bar included!
**This event is invite only, and you will recieve a confirmation email with additional details if selected to attend.
Life Science Backgrounds:
Clinical Data Programmer
Work with a Project Management team to setup, validate, and maintain clinical trial databases according to company standards; andAct as primary contact to the data management team for assigned studies, supplying all necessary technical support, and ensuring quality of the programming and adherence to company standards.No prior programming experience is required, as this training is provided once hired for the position. Data entry and data quality control experience a plus.Patient Recruitment Coordinator
Implement various recruitment strategies for clinical research studiesUpdate study specific social medica sitesTrack progress of media-generated referrals and overall study enrollmentRegulatory Submissions Coordinator
Communicate with research sites (doctor's offices, universities, hospitals, etc.) to collect all essential documents required before the site begins to screen patients to participate in the clinical trial;Maintain and perform ongoing quality review of trial documents within the Trial Master File (TMF);Collect, review, organize, and assemble regulatory start-up submissions (includes submissions to Institutional Review Boards)Data Coordinator
Validate an entry database design;Report metrics and data trends on project(s);Identify data conflicts and issues on project(s)Data Standard Analyst
Use SAS Programming to implement edit checks to reconcile data discrepancies and to create SDTM data that implements data standards Create annotated CRFs and mapping specifications per CDISC SDTM standardsPerform validation of CDISC SDTM data in accordance with SOPs and guidance documents, as well as ensuring data standard expected by regulatory agenciesProject Coordinator - CRO
Engage in clinical trial management on a day to day level;Work closely with the project CTM for timely delivery of recurrent tasks consistently with a high degree of accuracy;Coordinate project meetings and produce quality meeting minutes.
Clinical Research Associate
Travel 60-70% nationwide to clinical research sites;Conduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocol;Communicate with the medical site staff including coordinators, clinical research physicians, and their site staff.
Feasibility Coordinator
Strategize methodological plans for optimized study execution and performancePerform extensive research to make informed country and site selections
Proposal Writer:
Manage proposal development process for new businessStrategize content across science, finance, and operations
Informatics Analyst:
The informatics team utilizes informatics principles and techniques to architect, mine, analyze, and visualize clinical trial data to inform study design choices for pharmaceutical development. Informatics Analysts create compelling visualizations and recruitment models to support proposal feasibility strategies and ad hoc analytical projects.
All positions located in Cincinnati
Qualifications Bachelor's degree in Biology, Chemistry, Biomedical Engineering, Nueroscience, Math, or other Life Sciences Degree3.4 GPA or higherWilling to work in-office in Cincinnati, OH Medpace 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 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 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.
Cincinnati Perks
Cincinnati Campus OverviewHybrid work-from-home options (dependent upon position and level)Competitive PTO packages, starting at 20+ days Flexible work hoursDiscounted tuition for UC online programsCompany-sponsored employee appreciation events Employee health and wellness initiatives Community involvement with local nonprofit organizationsCompetitive compensation and benefits packageStructured career paths with opportunities for professional growthPartnership and discount with onsite childcare Discounts on local sports games, local fitness gyms and attractionsOfficial Sponsor of FC Cincinnati Modern, ecofriendly campus with an on-site fitness center, bar, and restaurants
Awards
Recognized by Forbes as one of America's Best Mid-size Companies in 2021, 2022 and 2023Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility
What to Expect Next
A 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