Dieses Jobangebot ist archiviert und steht nicht mehr zur Verfügung.
Vakante Jobangebote finden Sie unter Projekte.
Vakante Jobangebote finden Sie unter Projekte.
Top Opportunity for Statistical Programmers (Eng) - Brussels
Eingestellt von Clearsource
Gesuchte Skills: Support, Library, Unix
Projektbeschreibung
For one of my best clients I am actively looking for SEVERAL STATISTICAL PROGRAMMER for a challenging opportunity in a communicative company leader in its market. This is a long term assignment!
START: ASAP
DURATION: Full time - 10 months + possibility of extension
LOCATION: Brussels
DESCRIPTION:
As a Statistical Programmer you will:
- Support the analysis and reporting of clinical trial data for different departments and dossiers
- Derivation of new analysis variables in ADaM-like datasets initially developed to support Clinical Study Report deliverables
- Re-use and customization of existing analysis and reporting programs for creation of Table/Figures/Listings used in the different dossiers
- Development of new analysis datasets, original analysis programs and TFL macros as per specific requirements of various country specific reimbursement agencies.
- It could also consist in the finalization and/or validation of other filing deliverables like Integrated Safety Analysis, Statistical Review Aid, OSI packages,
SKILLS:
- At least 5 years of relevant clinical trial SAS experience in analysis and reporting.
- Proficient SAS PROGRAMMING skills with mastery of SAS/STAT SAS/BASE, SAS macro language. SAS/GRAPH is a nice to have. SAS/MACRO is a must for this mission.
- Capacity to interface with statisticians.
- Capacity to quickly read SAS code (including MACRO code) developed by others and understand them in the context of clinical trials.
- Knowledge and practice of CDISC SDTM AND ADAM DATA STANDARDS. ADaM is a must have.
- Ability to work complying to the company and project programming SOPs, project data standards and macro library as well as capacity to develop project specific code independently under company SOPs.
- Strong and proven experience of work with CLINICAL TRIAL DATA in support of safety and efficacy analysis.
- Prior Experience in supporting analysis and reporting deliverables for use in HTA dossiers is a real asset but not absolutely necessary.
- Fast learner, team oriented, able to work independently or under the guidance of a senior statistical programmer.
- Able to read, write and speak FLUENTLY IN ENGLISH.
- Experience with SAS on PC and UNIX platforms.
START: ASAP
DURATION: Full time - 10 months + possibility of extension
LOCATION: Brussels
DESCRIPTION:
As a Statistical Programmer you will:
- Support the analysis and reporting of clinical trial data for different departments and dossiers
- Derivation of new analysis variables in ADaM-like datasets initially developed to support Clinical Study Report deliverables
- Re-use and customization of existing analysis and reporting programs for creation of Table/Figures/Listings used in the different dossiers
- Development of new analysis datasets, original analysis programs and TFL macros as per specific requirements of various country specific reimbursement agencies.
- It could also consist in the finalization and/or validation of other filing deliverables like Integrated Safety Analysis, Statistical Review Aid, OSI packages,
SKILLS:
- At least 5 years of relevant clinical trial SAS experience in analysis and reporting.
- Proficient SAS PROGRAMMING skills with mastery of SAS/STAT SAS/BASE, SAS macro language. SAS/GRAPH is a nice to have. SAS/MACRO is a must for this mission.
- Capacity to interface with statisticians.
- Capacity to quickly read SAS code (including MACRO code) developed by others and understand them in the context of clinical trials.
- Knowledge and practice of CDISC SDTM AND ADAM DATA STANDARDS. ADaM is a must have.
- Ability to work complying to the company and project programming SOPs, project data standards and macro library as well as capacity to develop project specific code independently under company SOPs.
- Strong and proven experience of work with CLINICAL TRIAL DATA in support of safety and efficacy analysis.
- Prior Experience in supporting analysis and reporting deliverables for use in HTA dossiers is a real asset but not absolutely necessary.
- Fast learner, team oriented, able to work independently or under the guidance of a senior statistical programmer.
- Able to read, write and speak FLUENTLY IN ENGLISH.
- Experience with SAS on PC and UNIX platforms.
Projektdetails
Geforderte Qualifikationen
-
Kategorie:
IT Entwicklung, Sonstiges