Dear Allstat,
Please find below the latest permanent opportunity with Hays Pharma:-
Senior Statistical Programmer
Permanent
Global Pharma
Based in Switzerland (100% Client site)
Competitive salary
KEY RESPONSIBILITIES:
* Coordinate the programming activities for an individual phase I-II clinical trial or indication or small project, publication, or exploratory analysis under the supervision of the Program Programmer / Group Head.
* Lead the trial/indication/project team including resources planning and coordination of the different programming sites
* Make certain that study/indication/project documents and specifications are consistent and comply with company standards by providing input into Study protocol, CRF and Data structures and outputs (listings, tables and figures).
* Program according to specifications, analysis datasets, pooled datasets, listings, tables and figures for phase I-II clinical trials and for SCS and SCE with high quality and within milestones.
* Develop programming specifications for analysis datasets, pooled datasets and deliverables in consultation with the statistician.
* Develop and comply with project/study programming standards and specifications following internal guidelines.
* Support quality control and quality audit of deliverables.
* Participate as required at all meetings, discussions and activities covering aspects of Statistical Reporting on trial/indication/project level activities.
* Track clinical trial/indication/project milestones for statistical reporting deliverables.
* Maintain efficient interfaces with internal and external customers and communicate effectively across line functions.
* Mentor junior programmers
Minimum requirements
* University degree in Mathematics, Statistics, Data Analysis Program or Computer Science
* Ability to coordinate programming work across a clinical study.
* Must have experience using SAS in the analysis and the reporting of pharmaceutical data
* Working knowledge and expertise with SAS (including SAS macro language)
* Working knowledge of database design/structures
* Good understanding of global clinical trial practices, procedures and methodologies.
* Good understanding of regulatory requirements (e.g. GCP, ICH)
For a confidential consultation call Laura Christie on +44 207 633 4825 or email your CV to [log in to unmask]
I look forward to hearing from you.
Kind regards,
Laura
Laura Christie
Team Leader, Biometrics & HEOR, Europe
Recruiting experts in Life Sciences
HAYS Recruiting experts worldwide
25-27 Wootton Street
London
SE1 8TG
T: +44 207 633 4825
M: +44 7900 932031
F: +44 207 922 7101
E: [log in to unmask]<mailto:[log in to unmask]>
http://uk.linkedin.com/pub/laura-christie/18/492/6b9
hays.co.uk
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