Since our foundation in Dublin, Ireland in 1990, our mission has been to help our clients to accelerate the development of drugs and devices that save lives and improve quality of life. We do this by delivering best in class information, solutions and performance, with an unyielding focus on quality at all times. We offer a full range of consulting, development and commercialisation services from a global network of offices in 53 countries. We focus our innovation on the factors that are critical to our clients – reducing time to market, reducing cost, and increasing quality – and our global team of experts has extensive experience in a broad range of therapeutic areas.
Open Positions
Clinical Reserach Associate
Bachelor's degree in a scientific or healthcare-related field. 2+ years of experience as a Clinical Research Associate. In-depth knowledge of clinical trial processes and regulations
Senior Medical Writer
Advanced degree in Life Sciences, 3-5 years of experience in medical writing, proficiency in interpreting and summarizing complex clinical trial data
Clinical Data Coordinator
Bachelor's degree in Life Sciences or Healthcare, intermediate knowledge of clinical data management, familiarity with data management software
Statistical Programmer (All levels)
Bachelor’s or Master’s degree in Statistics, Mathematics, Computer Science, or a related field, experience in statistical programming, strong proficiency in SAS programming
Clinical Trial Manager
University degree in medicine, science, or equivalent combination of education & experience, 2+ years of experience in clinical trials, subject matter expertise in designated therapeutic area
Clinical Trial Assistant
Bachelor's degree in a scientific or healthcare-related field, prior experience or strong interest in clinical research, knowledge of clinical trial processes, regulations, and guidelines
Senior Medical Writer
Advanced degree in Life Sciences, 3-5 years of experience in medical writing, proficiency in interpreting and summarizing complex clinical trial data
CRA I, CRA II and Senior CRA
University degree, ICH-GCP knowledge, excellent communication skills, and ability to travel
Clinical Research Associate II/ Senior Clinical Research Associate
Advanced degree, Extensive experience as a Clinical Research Associate, Proven ability to manage multiple sites and projects simultaneously
Statistical Programmer II
Bachelor's degree in statistics or related field, experience as a statistical programmer, proficiency in programming languages such as SAS, R, or Python
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