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Statistical Programmer
Eingestellt von Montreal Associates
Gesuchte Skills: Library
Projektbeschreibung
Statistical Programmer
Duration: 6 months renewable to start in December
Location: Brussels
Your role
As part of our Brussels-based team, you coordinate statistical programming for the review, reporting and transfer of clinical trial data and in ADaM conversion projects.
TECHNICAL RESPONSIBILITIES
- Co-ordinate the creation of analysis dataset specifications in the ADaM standard, if needed.
- Co-ordinate the programming of analysis datasets, using specific SAS macros.
- Co-ordinate the creation of the metadata files (define.XML) using specific SAS macros.
- Ensuring traceability between SDTM and ADaM data.
- Co-ordinate the production of tables, listings & figures
- Co-ordinate the restructuring, review and integration of external data
- Co-ordinate the generation of consistency check programs and QC listings
- Co-ordinate the transfer of data according to customer specific requirements
- Develop adequately documented programs for the generation of randomisation schema/program
- Set & maintain professional programming standards
- Maintain & archive program documentation - both electronic & paper - in an appropriate manner
- Maintain awareness of current features & new developments in SAS
- Maintain professional programming standards
PROJECT RESPONSIBILITY & CUSTOMER INTERACTION
- Attend customer meetings to discuss project requirements/progress
- Understand scope of work, budget and scope assumptions
- Identify out of scope work & provide revised costs with supporting documentation
- Ensure project milestones are met to agreed timelines
YOUR PROFILE
- 2 to 8 years of relevant clinical trial SAS experience
- Proficient SAS programming skills with mastery of SAS/STAT SAS/BASE, SAS macro language. SAS/GRAPH is a nice to have
- Capacity to interface with clinicians, statisticians and data managers as statistical programmer in charge of a clinical trial
- Capacity to work independently or under the guidance of a senior programmer
- Ability to work complying to the company programming SOPs, data standards and macro library as well as capacity to develop project specific code independently under company SOPs
- Fluent English, written and spoken
Offer
We offer you the opportunity to be trained on the CDISC data standard with us as European leader in this domain.
Please apply and I will contact you for further information.
Duration: 6 months renewable to start in December
Location: Brussels
Your role
As part of our Brussels-based team, you coordinate statistical programming for the review, reporting and transfer of clinical trial data and in ADaM conversion projects.
TECHNICAL RESPONSIBILITIES
- Co-ordinate the creation of analysis dataset specifications in the ADaM standard, if needed.
- Co-ordinate the programming of analysis datasets, using specific SAS macros.
- Co-ordinate the creation of the metadata files (define.XML) using specific SAS macros.
- Ensuring traceability between SDTM and ADaM data.
- Co-ordinate the production of tables, listings & figures
- Co-ordinate the restructuring, review and integration of external data
- Co-ordinate the generation of consistency check programs and QC listings
- Co-ordinate the transfer of data according to customer specific requirements
- Develop adequately documented programs for the generation of randomisation schema/program
- Set & maintain professional programming standards
- Maintain & archive program documentation - both electronic & paper - in an appropriate manner
- Maintain awareness of current features & new developments in SAS
- Maintain professional programming standards
PROJECT RESPONSIBILITY & CUSTOMER INTERACTION
- Attend customer meetings to discuss project requirements/progress
- Understand scope of work, budget and scope assumptions
- Identify out of scope work & provide revised costs with supporting documentation
- Ensure project milestones are met to agreed timelines
YOUR PROFILE
- 2 to 8 years of relevant clinical trial SAS experience
- Proficient SAS programming skills with mastery of SAS/STAT SAS/BASE, SAS macro language. SAS/GRAPH is a nice to have
- Capacity to interface with clinicians, statisticians and data managers as statistical programmer in charge of a clinical trial
- Capacity to work independently or under the guidance of a senior programmer
- Ability to work complying to the company programming SOPs, data standards and macro library as well as capacity to develop project specific code independently under company SOPs
- Fluent English, written and spoken
Offer
We offer you the opportunity to be trained on the CDISC data standard with us as European leader in this domain.
Please apply and I will contact you for further information.
Projektdetails
Geforderte Qualifikationen
-
Kategorie:
IT Entwicklung