Product Manager

OverviewWe are seeking a dynamic and experienced Product Manager (Research Engineer) to lead the development and enhancement of our Core Lab Systems including Medical Imaging, Cardiovascular and Remote Biosensor Technology. This role will be pivotal in driving innovation and ensuring our platforms meet the evolving needs of our clinical trial sponsors. Responsibilities Product Vision & Strategy: Develop and communicate a clear product vision and strategy for Core Lab’s solutions, aligning with Medpace's overall objectives. Product Development: Drive end-to-end project execution, including planning, sprint management, and release cycles. Requirements Gathering & Prioritization: Collaborate with radiologists, clinical trial sponsors, and internal stakeholders to gather user needs and translate them into detailed product requirements. Prioritize features based on impact, feasibility, and alignment with business goals. Agile Methodology: Utilize Agile methodologies to manage product development, ensuring iterative progress and timely delivery of features. Cross-functional Collaboration: Work closely with software engineering, quality assurance, regulatory affairs, and other teams to ensure successful product development and launch. Regulatory Compliance: Ensure all Core Lab solutions comply with relevant regulatory standards and quality procedures. Stakeholder Management: Effectively communicate product updates and gather feedback from internal and external users. Qualifications Bachelor's degree in Computer Science, or a related field. Good experience as a Product Manager in the health care domain is preferred. Proven track record of launching successful applications. Experience with Agile/Scrum methodologies and tools like JIRA, Confluence, or Azure DevOps. Excellent communication and stakeholder management skills. Ability to translate complex user needs into clear and actionable requirements. Nice-to-have Strong understanding of medical imaging technologies and workflows in clinical trials. Knowledge of regulatory standards and quality procedures for medical devices and software. Experience with SQL databases, Angular, C#.NET. 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 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 NextA Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps. #J-18808-Ljbffr