At a Glance
- Tasks: Design and implement CDISC standards for clinical trials, ensuring compliance and efficiency.
- Company: Join IQVIA, a leader in clinical research and healthcare intelligence.
- Benefits: Enjoy a competitive salary, health benefits, and opportunities for professional growth.
- Other info: Collaborative environment with mentorship opportunities and career advancement.
- Why this job: Make a real impact on patient outcomes while working with innovative technologies.
- Qualifications: Bachelor's degree in a related field and experience with CDISC standards required.
The predicted salary is between 63000 - 77000 £ per year.
This position is responsible for the development of the end to end design of client standards and study specifications that align to the CDISC standards and regulatory agency guidance’s.
This position provides this guidance and training to clients of IQVIA.
Support clients and IQVIA as an authority in the use of CDISC Standards through communication, collaboration, training, and mentorship.
Partner with project statisticians and programming teams to develop global tools to support project programming needs in the use of CDISC Standards Lead the implementation of productivity tools for IQVIA and clients which improve compliance, efficiencies, and timeliness of deliverables to clients.
Provide training and mentorship for the use of technology and systems, such as metadata repositories, to support IQVIA and client’s in their use.
Assures that work delivered to clients meet minimum submission requirements as defined by FDA Guidance Documents and other regulatory guidance.
Monitors regulatory authority and standards organization sites for updates and informs IQVIA leadership of updates.
Bachelor's Degree in computer science, statistics, or a related area Experience with CDISC Standards, specifically SDTM and ADa MExperience on industry team involved in standards such as CDISC, HL7, or Transcelerate.
Strong communication skills10 years SAS programming experience or other related programming language experience preferred.
Knowledge and experience in two or more programming languages such as SAS, R, Python, Julia, C#, Java, or other language Relevant statistical programming experience with pharmaceutical clinical trial data preferred Experience in mentoring and developing others in the use of CDISC standards Experience in submissions to regulatory authority preferred IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.
We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.
Learn more at IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud.
Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law.
- Amsterdam, Netherlands
- Type: Full time
SAS Data Engineer in Reading employer: IQVIA
At IQVIA, we pride ourselves on being an exceptional employer, offering a dynamic work culture that prioritises innovation and employee well-being. Our South West England location provides flexible working arrangements, comprehensive well-being support, and robust career development opportunities through our AI-powered talent marketplace, ensuring that you can thrive both personally and professionally while contributing to meaningful advancements in healthcare.
