Director, Statistical Programming

CSL•King of Prussia, PA

19h

About The Position

The Director, Statistical Programming provides leadership and expertise in driving the development and maintenance of the CSL statistical programming capabilities which is required to meet regulatory obligations. Manages a team of programmers supporting clinical trial and integrated analyses, annual reporting, regulatory responses, publications, HTA requests and other purposes as needed within one or more therapeutic areas. The individual will work closely with the Senior Director, Clinical and Statistical Programming to advance the internal programming environment and statistical programming processes. Works closely with Statisticians to ensure that deliverables provided by internal resources or outside providers (CROs; FSP providers) are accurate and aligned with CSL standards.

Requirements

BSc in Computer Science, Mathematics, Statistics or related area with relevant experience
Other degrees and certifications considered if commensurate with related programming experience
At least 15 years of experience in the biotech, pharma, or CRO industries
Extensive understanding of clinical programming and/or statistical programming processes and standards
Advanced Experiences with statistical programming using the SAS software including development and use of SAS Macros, preferred managing team performing these activities as well
Advanced knowledge in CDISC standards (CDASH, SDTM, ADaM)
Proven ability to work effectively both independently or in a team setting, and to meet set goals by managing own timelines
Experience in working in cross-functional, multicultural and international clinical trial teams
Coding in SAS, including SAS macro language
Strong interpersonal and communication skills (verbal and written in English), comfortable around senior management
Ability to collaboratively work and provide leadership in matrix environment
A solutions oriented mindset
Fluency in technical requirements for CDISC compatible datasets and DDT files

Nice To Haves

Preferred 5 or more years of direct supervisory experience
Experience with CRO management and/or CRO work experience
Interest and/or experience in expanding beyond SAS as the primary programming delivery tool
Experience in and passion for automatization of routine programming tasks
Broad knowledge of clinical development and processes
Presentations of programming techniques at professional conferences is a plus

Responsibilities

Working with the Biometrics Programming Leadership team, assess upcoming activities and resulting resource needs and allocate projects to people to ensure high quality, timely, delivery. Ensure realistic resource planning.
Oversee the CRO delivery or manage the in-house programming of data sets, outputs, and DDT files of clinical trials and integrated analysis.
Coordinating the oversight or in-house programming of exploratory analyses, analyses to support secondary publications, response to regulatory requests, or other adhoc requests.
Manages, hires, and mentors direct reports including annual evaluations and goal setting.
As a member of the programming leadership team within biometrics, creates, maintains ensures compliance with programming process and strategy to facilitate accurate and timely analysis programming.
Help bring state of the art programming methods and tools to the organization and drive automation of delivery, including AI.
Collaborate with Biometrics and other departments to ensure transition points in process are efficient and of high quality.
Represents the company in outside professional organizations and meetings.