Clinical Informatics Analyst

Job Summary Medpace is expanding a new Clinical Informatics team and is looking for qualified individuals to support this initiative. Our analysts work directly with Clinical Operation teams to identify needs and establish solutions spanning data analytics, visualization, and accessibility. Analysts will be trained to evaluate study protocols and work collaboratively with Clinical Trial Managers to develop and validate data products that increase operational efficiency.

Analysts will support both custom- and enterprise-wide solutions as they work hand-in-hand with our software engineering teams.

Responsibilities Evaluate data needs for assigned projects and make recommendations on strategic approach specific to the study design;

Work alongside operational and medical leads to contribute innovative data products;

Interact with relational data at both study- and enterprise-level inclusive of actions for query, wrangling, analysis, and reporting;
Innovate algorithms to describe, classify, and predict operational outcomes of clinical trials; and Support departmental process improvement initiatives.

Qualifications Qualifications Bachelor ’s in informatics, computer science/engineering, biomedical engineering, health information, statistics, or related field;

Analytical thinker with great attention to detail;

Ability to prioritize multiple projects on a sprint schedule;

Excellent verbal communication skills;

Programming experience in R or Python;

Work experience with clinical data;

Experience building web applications is preferred (with either Shiny or Streamlit); and Experience building dashboards is preferred (with either PowerBI, Tableau, or Spotfire).Additional Considerations We are hiring all levels of experience. Degree level, work experience, interview performance, and programming proficiency will be considered. Prior to the interview stage, a programming assessment will be conducted, details will be shared with candidates during scheduling confirmation.

Medpace Overview Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV 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 the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective.

Headquartered in Cincinnati, Ohio, we employ more than 6,500 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, creative thinking, and continuous learning through open communication and mutual trust.

Leadership throughout Medpace is both accessible and approachable

Continuous Growth & Development Office based environment with on-site mentors

Defined career paths with clear advancement opportunities

Industry renowned onboarding and training programs designed to accelerate professional development

Ongoing training and continuous learning opportunities throughout your career

An environment that encourages employees to influence…