A CRO that provides statistical programming to pharmaceutical, biotechnology, and medical device companies is looking to hire an Associate Director Statistical Programmer that is responsible for directing, leading, and managing a team of statistical programmers to deliver the requirements of the drug product. You will be an integral part of the Statistical Programming department that manages and produces the programming attributes for several clinical studies.
The Associate Director Statistical Programmer will be responsible for:
- Represent the Statistical Programming team to report deliverables and focused timelines
- Act as strategic programming leader providing support to clinical trials, developmental plans, clinical plans, proposals, and commercialization
- Manage stipulations of expertise to external affiliates in design and distribution of STDM, ADaM, SAP, CDISC
- Create program design processes consistent with business procedures
- Support in development of training and onboarding statistical programmers
- Develop or enhance SOP's and Work Instructions for statistical programming
The Associate Director Statistical Programmer should have the following qualifications:
- Bachelors Degree in Statistics, Mathematics, Computer Science, Life Sciences or other pertinent scientific fields; Masters Degree preferred
- 10+ years of experience in developing software using SAS for clinical trials
- Exceptional understanding of statistics and drug development
- Excellent knowledge of CDISC standards, including SDTM and ADaM models
- Proven competence and experience for project management of statistical programming designs
- Proven leadership capability to efficiently control statistical programming activities and incorporate them with the complete clinical operation
- Customer- and quality-focused, detail oriented, and exceptional teamwork abilities
- Strong organizational and time management skills
If you are interested in the Associate Director Statistical Programmer role, then please don't wait to apply.