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IQVIA Inc is seeking an Associate Statistical Programming Director to lead and support statistical programming efforts within clinical development. The role involves ensuring the accuracy and regulatory compliance of clinical data while managing a small team and collaborating across various departments.
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Job Summary
Responsible for providing leadership and hands-on support in the development and maintenance of statistical programming capabilities to meet regulatory obligations.
Leads and oversees the design and implementation of complex SAS programs for applications designed to analyze and report complex clinical trial data in CDISC ADaM format.
Provides leadership to a team of direct reports to drive their development, efficiency, innovation and career progression.
Matching Summary
Match Score: 75
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IQVIA Inc is seeking an Associate Statistical Programming Director to lead and support statistical programming efforts within clinical development. The role involves ensuring the accuracy and regulatory compliance of clinical data while managing a small team and collaborating across various departments.
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Salary
Base: $98,200.00 - $273,200.00; Bonus/Equity: Incentive plans, bonuses may be offered; Benefits: Range of health and welfare and/or other benefits
Skills & Requirements
Must-have
SAS programming
CDISC SDTM and ADaM
submission ready data
clinical trial data analysis
regulatory requirements
Nice-to-have
leadership and hands-on support
process improvement initiatives
cross-functional collaboration
solutions-oriented mindset
networking and knowledge sharing
Key Requirements
10+ years experience in clinical/statistical programming
Experience in CRO/pharmaceutical environment
Proven experience leading programming for pooled/exploratory analyses
BSc in Computer Science, Mathematics, Statistics or related area