Statistical Programmer
- Employer
- RBW Consulting
- Location
- Germany (DE) or France (Remote Working)
- Salary
- 60000 -80000
- Start date
- 28 Sep 2021
- Closing date
- 28 Oct 2021
View more
- Discipline
- Data Management / Statistics, Statistical Programming
- Hours
- Full Time
- Contract Type
- Permanent
- Experience Level
- Experienced (non-manager)
Job Details
Senior Statistical Programmer
Ashley Clarke @ RBW consulting is currently recruiting for a Senior SAS Programmer to work for a European CRO. They work with industry leaders with in Pharmaceuticals and in turn are looking for dedicated professionals to maintain their high standards and reputation within the industry.
I am looking for experienced SAS Programmers that are interested and would thrive working in a FSP team. You will be working closely with the sponsor and embedded into their systems.
Senior SAS Programmer
Responsibilities
As a Senior Programmer:
- Programming of analysis datasets and TLFs for reporting and analysis of clinical trials.
· Development of programs to merge study data in different data formats into an integrated
database for regulatory approvals.
· Responsible for QC and validation of SAS programs.
· Program SAS standards for projects and studies.
· Conception, development, documentation and validation.
Job Profile
- Develop SAS programs for generating datasets, tables, figures and listings for clinical trials (according to ICH E3) and/or publication and/or Health Authorities requests;
- Be the CDISC SDTM/ADaM expert; use CDISC guidelines to generate SDTM/ADaM datasets; - Develop standard SAS macros and prepare the corresponding validation documents;
- Perform quality check on SAS programs/outputs created by another Statistician/SAS Programmer; - Develop SAS programs/macros and utilities for data cleaning; - Liaise with Data Management team in identifying and implementing checks according to the Data Validation Plan;
- Check the requirements to handle external clinical data and develop the SAS programs to import/reconcile external clinical data;
- Develop and validate SAS programs for identification of Protocol Deviations; - Establish and implement programming rules;
Qualifications
· University degree in the field of natural sciences, statistics or mathematics (Bachelor required,
Master of advantage).
· Several years of professional experience as a statistical programmer in the pharma sector.
· CDISC knowledge.
· Experience in submission (FDA).
· Profound programming skills in SAS 9.x in the BASE, STAT, GRAPH module.
· Good SAS macro and SQL programming skills.
· Solid statistical knowledge.
· Very good analytical and conceptual skills.
· Fast grasping, good implementation and independent operation.
· Very good English skills in spoken and written English.
· strong team and communication skills.
· SAS certifications are of benefit but not essential.
To find out more about this fantastic opportunity or to discuss other open positions which may be of interest please contact Ashley Clarke on +44 (0) 1273 952 363 and send your CV through using the apply button on this page.
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