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 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 change, contribute ideas, and grow quickly
Other Employee Benefits
Competitive compensation programs that recognize and reward performance
Comprehensive health, wellness, retirement, and PTO benefits
Office based culture with occasional WFH that provides flexibility for eligible positions after training
Company-sponsored social events
Please note benefits may vary based on country.
What to Expect Next
A Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted.
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.
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)
