ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.
We are currently seeking a Senior Clinical Data Science Programmer to join our diverse and dynamic team. As a Senior Clinical Data Science Programmer at ICON, you will play a pivotal role in developing and implementing programming solutions to support the analysis and reporting of clinical trial data. You will contribute to the advancement of innovative treatments and therapies by ensuring the accuracy and efficiency of data processing through your programming expertise.
What You Will Be Doing:
Develop, validate, and maintain programming solutions for CDMS (EDC systems such as Rave/Veeva), data validation outputs, data review/risk management outputs, custom reports, and programs in clinical trials.
Collaborate with data managers, project managers, clinical data scientists, and biostatisticians to ensure the integration of programming solutions into the overall data management process.
Act as a primary point of contact during the study set up and maintenance phase for system programming related questions by the project team.
Support colleagues with the clinical trials environment and concepts of Clinical Data Management Systems.
Perform extracts of data from CDMS and creation of data transfer programs.
Act as mentor and provides guidance and support to more junior programmer levels assigned to a project.
Assist in the development and implementation of improvements to technical systems and processes within an SME role.
Provide guidance on programming best practices, coding standards, and data quality control measures.
Stay updated on advancements in programming languages and data management tools to enhance operational efficiencies.
Your Profile:
Complete bachelor’s degree relevant field such as computer science, SAS, statistics, or life sciences.
Extensive experience in programming for CDMS (EDC systems such as Rave/Veeva), data validation outputs, data review/risk management outputs, custom reports, and programs in clinical trials with proficiency in languages such as SAS, R, or Python.
Strong problem-solving skills and the ability to work collaboratively in a fast-paced, cross-functional environment.
Excellent attention to detail and organizational skills, with a commitment to delivering high-quality results.
Strong communication and interpersonal skills, with the ability to effectively collaborate with diverse teams and influence outcomes.
MUST HAVE advanced English Communication, Writing and Reading
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Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
Rewards & Benefits
ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.
Benefits may include:
Benefits may vary depending on role and location.
Visit our careers site to read more about the benefits ICON offers.
Inclusion and Accessibility
ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.
If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.
Are you a current ICON Employee? Please click here to apply
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