IT Software Development Project Manager

We are seeking an experienced IT Project Manager to join our Information Technology team. In this role, you will lead the planning, execution, and delivery of custom software projects that support our clinical and business operations. You'll work closely with developers, business stakeholders, and IT leadership to ensure our internally developed software solutions are delivered on time, within scope, and aligned with organizational goals.

Lead end-to-end project management for custom software development initiatives, from initiation through deployment and post-launch support; Develop and maintain detailed project plans, timelines, and resource allocation schedules; Facilitate communication between IT development teams, business stakeholders, and executive leadership; Define project scope, goals, and deliverables in collaboration with stakeholders and technical teams; Identify, track, and mitigate project risks and issues, escalating as appropriate; Manage project documentation, including requirements, status reports, and change requests; Coordinate sprint planning, stand-ups, and retrospectives for teams using Agile/Scrum methodologies; Ensure software development projects comply with relevant regulatory, quality, and data integrity standards (e.g., GxP, 21 CFR Part 11, SOx); Support change management and user adoption efforts for newly deployed software, including working with the business to run pilot studies; and Conduct post-project reviews to capture lessons learned and improve future project delivery.

Required: Bachelor's degree in Information Technology, Computer Science, Business Administration, or related field (or equivalent experience); 3+ years of experience managing IT or software development projects; Strong understanding of software development lifecycle (SDLC) methodologies, including Agile; Excellent verbal and written communication skills, with the ability to translate technical concepts for non-technical stakeholders; Proficiency with change management tools (e.g., Microsoft Azure DevOps); Strong organizational skills with the ability to manage multiple concurrent projects; and Demonstrated experience managing project timelines and cross-functional teams. Preferred: PMP, CSM, or other relevant project management certification; Experience working in a Contract Research Organization, pharmaceutical, biotech, or other regulated life sciences environment; Familiarity with regulatory requirements such as GxP, 21 CFR Part 11, HIPAA, or SOx; Experience managing custom software development projects (rather than only vendor/COTS implementations); and Working knowledge of software development concepts sufficient to engage credibly with engineering teams. 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? 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 Work Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence   Collaborative Culture Contribute to an interactive team environment that empowers decision making,