At a Glance
- Tasks: Design and implement client standards aligned with CDISC guidelines while mentoring and training clients.
- Company: Join IQVIA, a leader in clinical research and healthcare intelligence.
- Benefits: Competitive salary, professional development, and opportunities for global impact.
- Other info: Dynamic role with opportunities to lead and innovate in the life sciences sector.
- Why this job: Make a difference in healthcare by ensuring compliance and improving efficiencies.
- Qualifications: Bachelor's degree in a related field and experience with CDISC Standards required.
The predicted salary is between 60000 - 80000 £ 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. This position provides this guidance and training to clients of IQVIA.
Job Responsibilities:
- 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 clients in their use.
- Assure that work delivered to clients meets minimum submission requirements as defined by FDA Guidance Documents and other regulatory guidance.
- Guide clients in their use of CDISC standards through governance teams.
- Monitor regulatory authority and standards organization sites for updates and inform IQVIA leadership of updates.
- Work on other IQVIA initiatives as a CDISC representative.
- Interact with various CDISC sanctioned teams in the development of standards.
- Represent IQVIA in the industry as a leader in the use of Standards and Automation.
- Support leadership in the development of processes and tools which enable CDISC compliance.
Minimum Requirements:
- Bachelor's Degree in computer science, statistics, or a related area.
- Experience with CDISC Standards, specifically SDTM and ADaM.
- Experience on industry team involved in standards such as CDISC, HL7, or Transcelerate.
- Strong communication skills.
- 10 years SAS programming experience or other related programming language experience preferred. Knowledge of macro or subroutine development is expected.
- 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.
Data Standards Engineer (CDISC) employer: IQVIA
IQVIA in Livingston, Scotland is an excellent employer that fosters a collaborative team environment and prioritises employee growth through outstanding career development opportunities. Working as a Lab Operations Assistant here not only allows you to contribute to meaningful projects but also ensures you are part of a supportive workplace that values safety and professionalism.
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We think you need these skills to ace Data Standards Engineer (CDISC)
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