As a Clinical Data Programmer you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
What you will be doing:
- Review and apply data mappings for customer specific data exports
- Perform peer review / QC of data export programming
- Produce data transfers via data export files and/or web services
- Work with customers to specify data transfer standards and develop/implement software code to automate data transfer activities
- Provide database programming support for custom reports
- Perform peer review / QC of custom report programming
- Create and implement database scripts to correct issues
- Participate in departmental discussions regarding technical, functional and process improvement
- Ensure that all project-related programming tasks are completed in accordance with standard practices throughout the lifecycle of the project including, but not limited to:
- Perform data integration configuration, programming, and documentation
- Process Data Clarification Forms (DCFs)
- Manage and program targeted rules
- Oversee data outputs for integrity and accuracy
- Triage, research and provide solutions for identified data issues
- Communicate progress and roadblocks on programming efforts to internal and external stakeholders
- Assist junior staff to troubleshoot programming issues
- Contribute to department knowledge share for common issues, standard processes, guides, etc.
You are:
- Bachelor’s degree in computer science, software engineering, information technology, informatics, or closely related field
- 5+ years of experience as a software developer, database analyst/programmer, or clinical software tester
- 5+ years of experience with programming in Microsoft SQL, MySQL, Snowflake, or other related databases
- 5+ years of experience building reports in SSRS, Logi, PowerBI, Tableau or other reporting tools
- 3+ years of experience programming in SAS
- 5+ years of experience with Clinical Data Management and clinical development technology solutions
- Understanding of the clinical trial processes, including common data standards (CDISC) and Study Data Tabulation Model (SDTM)
- Ability to manage competing priorities and can work in a dynamic environment
- Comfortable writing and troubleshooting complex SQL queries that include PIVOT, Indexing, CTE’s, Subqueries, etc.
Why ICON?
Our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.
Our success depends on the knowledge, capabilities and quality of our people. That’s why we are committed to developing our employees in a continuous learning culture – one where we challenge you with engaging work and where every experience adds to your professional development.
ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know.
Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.
