The Principal Statistical Programmer will be recognized as a subject matter expert, providing technicalsupport and expert advice to internal and external sponsors, and works independently to support variousprograming activities related to the analysis and reporting of clinical study data.
In addition, the PrincipalStatistical Programmer can fill the Statistical Programming Lead role on projects and liaise with sponsors,Biostatistics Leads, Data Management Leads, and other functional areas as required.
Further, thePrincipal Statistical Programmer will monitor quality, timelines, resource allocation, and productivity inrelation to budgets.
QualificationsExcellent analytical skills with sound Lead experience as a Senior Statistical Programmer within the Clinical Research (CRO) environment.
Advanced knowledge of SAS programming techniques.
Extensive knowledge and understanding of the programming and reporting process.
Good knowledge of SOPs / Guidelines, ICH-GCP, and any other applicable local and internationalregulations such as 21 CFR Part 11.
Knowledge of the efficacy endpoints and analysis techniques specific to the disease beingtreated.Ability to learn new systems and function in an evolving technical environment.
Strong project management skills.
Strong organizational skills, ability to manage competing priorities, and flexibility to change.
Attention to detail.
Ability to successfully lead and mentor a global team.
Work effectively in a quality-focused environment.
Excellent time management in order to meet daily metrics or team objectives.
Show commitment to and perform consistently high quality work.
Strong business / operational skills that include customer focus, commitment to qualitymanagement, and problem solving.
Demonstrate commitment to refine quality processes.
Good presentation skills.
Ability to negotiate and influence in order to achieve results.
Good business awareness / business development skills (including financial awareness).
Client-focused approach to work.
Good negotiation skills.