Clinical Database Designer

Job Summary Our global activities are growing rapidly and we are currently seeking a full-time office-based Clinical Database Designer to join our Biometrics team This position will work in a team to accomplish tasks and projects that are instrumental to the company s success If you want an exciting career where you use your previous expertise and can develop and grow your career even further then this is the opportunity for you Responsibilities Maintain eCRF and Edit Check Specification standard templates according to CDISC standards for data collection and data submission Develop and maintain eCRF specifications on a study-by-study basis e g reviewing protocol and customize library eCRFs to apply for the study from database build through database lock including Change Requests Develop and maintain Edit Check Specifications from database build through database lock including Change Requests to ensure that all data collected are present logical and per expected protocol assessment schedule and completion guidelines Perform validation of both the eCRF and the edits per the specifications ensuring that all possible entry scenarios are tested and documented Accountable for providing reliable and concise feedback to clinical data programmer Liaise and educate the Data Manager and Sponsor to ensure that eCRFs are well understood and the EDC database is set up per Sponsor expectations e g attend ongoing meetings with the Sponsor during setup of study Liaise with Clinical Db Programmer to ensure that eCRF and Edit Check Specifications are clearly defined and can be accomplished in the referenced system Design and develop customized project-level reports that are useful to the team via the reporting tools within the EDC systems e g Business Objects JReview Lead eCRF specification review meetings with internal project team to discuss eCRF specifications and Lead eCRF specification review meetings with external project team to discuss eCRF specifications and speak knowledgeably about decisions made and technical design options if Sponsor does not agree with current design Qualifications Bachelor s degree Advanced degree in Life Sciences or Computer Science or equivalent At least one year experience building specifications and or performing UAT for EDC databases Excellent verbal and written communication skills and Meticulous attention to detail 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 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 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 Perks Flexible work environment Competitive compensation and benefits package Competitive PTO packages Structured career paths with opportunities for professional growth Company-sponsored employee appreciation events Employee health and wellness initiatives Awards Recognized by Forbes as one of America s Most Successful Midsize Companies in 2021 2022 2023 and 2024 Continually 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