We are seeking a highly skilled Statistical Programmer to join our team at IQVIA. As a Statistical Programmer, you will utilize the SAS programming language to develop clinical study report materials according to the objectives of a clinical trial for regulatory submissions.
Responsibilities:
* Import data from various sources.
* Program quality control checks for source data and reporting data issues.
* Interpret project level requirements and develop programming specifications.
* Write programming code following established Good Programming Practices.
* Program SDTM and ADaM datasets.
* Program to create statistical analysis tables, listings, and figures.
* Validate datasets and all statistical outputs per prescribed gate checks.
* Communicate with internal and client statisticians and clinical team members to ensure appropriate understanding of requirements and timelines.
* Use and promote the use of established standards, SOPs, and standard methodologies.
* Export data and clinical study report materials.
* Provide training and mentoring to team members and department staff.
You will have the opportunity to bring clinical trial statistical analysis into the next generation. Our team is award-winning and innovative, and we offer access to cutting-edge in-house technology, allowing you to work on global projects across therapeutic areas.
The Ideal Candidate
We are looking for candidates with a Master's or Bachelor's degree in Biostatistics, Statistics, Mathematics, or Computer Science, and who have a strong educational or practical background in programming.
Key Requirements:
* 5+ years of experience in a Statistical Programmer role from CRO/Pharma with ADaM/SDTM/TFLS.
* Excellent accuracy, attention to detail, problem-solving, organizational, and interpersonal communication skills.
* Experience in programming in SAS within the CRO/Pharma/Biotech/Healthcare industries.
* Knowledge of statistics and routine and occasionally complex analytical skills.
* A focus on quality, accuracy, and completeness of work activities.
* Excellent communication skills.
* A good understanding of Good Clinical Practice and ICH guidelines.
* Ability to independently lead and estimate programming scope of work, handle resource assignments, communicate work status, and work within project timelines for deliverables.