Job Title

Manager, Statistical Programming

Salary

£30,000 - £45,999

Job Type

Databases/Programming, It/System Validation, Project Control/Budgets, Programming, Statistics

Location

Essex/Hertfordshire

Employment Type

Permanent Job With CSL Or Client

Employer Type

PM Pharmaceutical R&D HQ (Global Or EU)

Seniority

Team Manager/Project Manager

Duration

 

FTE Hours

Full Time 35 - 40hrs Per Wk

Vacancy Status

Open For Applications

Date Posted

Mon 14th July 2008, 03:05pm

Are you an experienced Statistical programmer with Project management experience seeking a role within a leading Global Pharma?

Our client are a Japanese Global Pharma who is committed to developing and delivering healthcare products that truly benefit humanity and responds to the diverse healthcare needs of people around the world. Our client works globally on three main therapeutic areas: CNS, Gastro-Intestinal and Oncology. They are now looking to recruit a Statistical Programming manager to join their team on a permanent basis based in Hertfordshire.

The purpose of this role would be to support the Biostatistics team by carrying out statistical programming work and providing statistical programming and validation support forboth internal and external EGC projects. Operates as an effective team member, demonstrating the ability to work efficiently and to a high standard within a clinical team environment. Contributes to the overall efficiency and best practice running of^the Biostatistics group, demonstrating the ability to work efficiently and to a high standard within a clinical team environment. Providing statistical programming and validation support for analysis datasets, statistical tables, figures, listings,patient profiles, SAS transport files, Integrated Summaries of Safety (ISS), electronic submissions, related clinical trials and for other internal and external requests (e.g., publications). Working with external vendors in order to develop or monitor the content and structure of SAS datasets, when necessary.

Qualifications and Skills required:

Bachelor's degree in associated functional discipline and MSc (biostatistics, statistics or computer science).
Experience in SAS programming for phase I-IV clinical trials in a pharmaceutical/CRO environment.
Some project or people management experience in a pharmaceutical/CRO programming environment or demonstrated significant leadership of SAS programming activities in a clinical pharmaceutical/CRO environment.