Beschreibung
For our pharmaceutical client in Basel, we are looking for an experienced
SAS Programmer
Start:
End:
Location: Basel
Your main task will be the following:
"Project/Compound" related work:
* Program according to specifications, analysis datasets, pooled datasets, listings, and figures for clinical trials and submission activities
* Support quality control and quality audit of deliverables
* Maintain records for all assigned projects and archiving of trial/project analysis and associated documentation
"Standard Programming" related work:
* Develop Oncology Generic Programming Code according to specifications, following internal guidelines
* Reinforce & Implement programming standardization
* Enhance programming environment & systems
* Manage the testing of macros by setting and performing Test scripts
* Write any documentation for standard macros uses (eg user manual).
* Maintain efficient interfaces with internal and external customers and communicate effectively across line functions.
* Coordinate programming activities across several trials with a given compound including publication and regulatory submission activities.
* Provide input as required at all meetings, discussions and activities covering aspects of Statistical Reporting on trial level activities
* Track clinical trial milestones for statistical reporting deliverables.
Skills Required:
* Proven experience using SAS in the analysis and the reporting of pharmaceutical data
* Working knowledge of database design/structures
* Extensive Knowledge of SAS including Base, Macro, Stat, ODS etc
* Knowledge of CDISC data standards
* At least 4 years experience in Pharmaceutical SAS Programming
* Experience in Oncology therapeutic area
* Experience across all Phases of trials and Submissions
* Effective team player but also comfortable with autonomy
* Fluent English
Kinldy send your CV
Beheshta Saya
Michael Bailey International is acting as an Employment Business in relation to this vacancy.