Experienced Informatics Analyst

We are currently seeking an experienced informaticist to join our Informatics team who will lead advanced analyses of methodological data to inform study design decisions. 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. The informaticist will create predictive data models to identify and analyze patterns, then program compelling visualizations of the data to support feasibility strategies.

The team is seeking an experienced candidate for a senior‑level position to contribute new skills, support team growth, and foster fellow analyst development.

The Informatics Team is highly collaborative with members in both the Cincinnati and London offices. It supports clinical operation, medical, and feasibility teams with advanced data query and analysis and works alongside business analytics and software engineering to architect innovative data storage and access solutions.

• Utilize advanced statistical methods to develop predictive algorithms of methodological and clinical data.
• Translate the results of feasibility research and analysis into compelling data visualizations that illustrate the overall feasibility strategy.
• Perform comprehensive review of data sources to deliver high‑quality informatics data and analysis to teams.
• Develop and map database architecture of methodological and clinical data systems.
• Work alongside global feasibility leads to contribute to proposal strategy for site and country selection based on available data.
• Assist project teams with preparation for bid‑defense meetings.
• Support departmental process‑improvement initiatives.

• Master’s degree in informatics, computer science/engineering, health information, statistics, or related field required;
  Ph.D. preferred.
• Advanced computer programming skills (preferred language: R).
• Analytical thinker with great attention to detail.
• Ability to prioritize multiple projects and tasks within tight timelines.
• Excellent written and verbal communication skills.
• Participation in training and development of more junior team members.

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. Medpace accelerates global development of safe and effective medical therapeutics through a scientific and disciplined approach, leveraging local regulatory and therapeutic expertise across major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti‑viral and anti‑infective. Headquartered in Cincinnati, Ohio, Medpace employs over 5,000 people across 40+ countries.

People, purpose, passion. Make a difference tomorrow. Join us today. Our work over the past 30+ years has positively impacted countless patients and families and will continue to improve lives worldwide.

• 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.

• 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.

A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.

Not Applicable

Full‑time

Engineering and Information Technology

Pharmaceutical Manufacturing