Latest Job Recruitment at ICON plc
Job Title: SAS Programmer II
ICON plc is the best organization in the world for healthcare intelligence and clinical studies. From molecules to medicines, we advance clinical research by offering outsourced services to pharmaceutical, biotechnology, medical device, government, and public health organizations. We help speed up the development of drugs and devices that save lives and make people’s lives better by putting our patients at the center of everything we do.
People are our biggest strength, the heart of our society, and the reason we’re successful. ICON people are driven to achieve and have a passion for what they do, which helps them do it well.
Responsibilities
- All SOPs, WIs, policies, and local legal requirements will be followed when services are provided.
- Offers experience in planning, making, and overseeing clinical programming activities and deliverables, from setting up a study to making CDISC SDTM tabulation packages (aCRF, define.xml, cSDRG, etc.) ready for submission.
- Review all the paperwork for setting up the trial and give your thoughts on it.
- It is their job to look over or make aCRF, DTA metadata, and trial design specs.
- Make or review internal data and/or SDTM mapping requirements
- Use the internal conversion structure, utilities, and global checks to make or look over internal data and/or SDTM datasets.
- Make sure that all datasets are reviewed for quality (e.g., by checking for Pinnacle 21 compliance); make sure that datasets can be used by stakeholders (for medical review, central tracking, adaptive design, etc.); and make sure that datasets are compliant for both the interim and final databases.
- Quality review checks and reports for Data Managers and other team members can be programmed, or someone can be in charge of creating them.
- Responsible for making ready-to-submit SDTM packages for the FDA/PMDA or other regulatory authorities and staying up-to-date on regulatory changes.
- It is their job to learn and keep up-to-date on the different data collection tools used in clinical trials, like Medidata Rave, Clinical Data Tools like LSAF and Pinnacle 21, and CDISC standards like SDTM, CDASH, Controlled terms, and XML.
- Help create standards and make sure they are followed by everyone in the company.
Requirements
- Clinical programming experience and/or experience
- A Bachelor’s degree or higher in computer science, data science/data engineering, mathematics, or another related scientific area (or an equal level of theoretical and technical depth).
- Expertise in writing with SAS, Define.xml, SDTM aCRF, and SDGs.
- Expertise in data structures (like CDISC SDTM and ADaM) and how to use them.
- Experience working in cross-functional, global, and multiregional teams with people from many different backgrounds in clinical research.
- Project control skills.
- Very well planned and able to communicate well both in writing and in person.
How to Apply for this Job Recruitment at ICON plc
Closing Date: 28th June 2023
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