Senior Statistical Programmer - Oncology (m/w/d)
IQVIA is looking to appoint statistical programmers to utilize the SAS programming language to develop clinical study report materials according to the objectives of a clinical trial for regulatory submissions. Programming and performing related tasks serving the full spectrum of statistical programming needs in our DS3 environment (home based).
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, listing 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
We offer access to cutting-edge in-house technology and opportunities to work on global projects across therapeutic areas. You will be challenged in a fast-paced, collaborative biostatistical analyses and advanced statistical programming environment. Development opportunities and mentoring are available to help you progress in your long-term career.
The Person
Candidates should possess a Master’s or Bachelor’s degree in Biostatistics, Statistics, Mathematics, or Computer Science, and have strong educational or practical experience in programming.
Key required skills
* Home Based/Remote
* 5+ years of experience in a Statistical Programmer role from CRO/Pharma with ADaM/SDTM/TLFs
* Excellent accuracy, attention to detail, problem solving, organizational and interpersonal communication
* Experience in SAS programming within CRO/Pharma/Biotech/Healthcare industries
* Knowledge of statistics and routine to occasionally complex analytical skills
* Focus on quality, accuracy, and completeness of work activities
* Excellent communication skills
* Understanding of Good Clinical Practice and ICH guidelines
* Ability to independently lead (or have lead potential) and estimate programming scope of work, manage resource assignments, and meet project timelines
* Proactive, reliable, and able to work with integrity
* Ability to establish and maintain effective working relationships with co-workers, managers, and clients
This role is not eligible for UK visa sponsorship
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. Learn more at https://jobs.iqvia.com
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