Feasibility Informatics Analyst

Job Summary The Feasibility & Proposals department is looking for qualified analysts to join our Informatics Team in our London office. The informatics team utilises informatics principles and techniques to architect, mine, analyse, and visualise clinical trial data to inform study design choices for pharmaceutical development. Informatics Analysts create compelling visualisations and recruitment models to support proposal feasibility strategies and ad hoc analytical projects.

The Informatics Team is a highly collaborative team with members in both the Cincinnati and London offices. This team supports clinical operation, medical, and feasibility teams with advanced data query and analysis. The Informatics Team also works side-by-side business analytics and software engineering to architecture innovative data storage and access solutions for optimal data utilisation strategies. If you are an individual with a background or interest in data science, statistics or epidemiology, please review the following career opportunity.

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

Perform comprehensive review of data sources to deliver high quality informatics data and analysis to teams;

Work alongside global feasibility leads to contribute to proposal strategy for site and country selection based on available data;

Translate the results of feasibility research and analysis into compelling data visualisations which illustrate the overall feasibility strategy including enrolment modelling;

Design and implement database architecture plans and perform custom queries for methodological and clinical data sources;

Perform development and review of proposal text;

Assist project teams with preparation for bid defence meetings; and Support departmental process improvement initiatives.

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

Analytical thinker with great attention to detail;

Ability to prioritise multiple projects and tasks within tight timelines;

Excellent written and verbal communication skills;1-2 years of clinical research experience is preferred; and Computer programming experience for data queries, database structure, and/or statistical analysis (preferred language: R)
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…