Description
This statistical programmer will support the analysis and reporting of clinical trial data for Health Technology Assessment purposes. This includes the derivation of new analysis variables in ADaM-like datasets initially developed to support Clinical Study Report deliverables. It includes re-use and customisation of existing analysis and reporting programs for creation of Table/Figures/Listings used in HTA dossiers. It may also include development of new analysis datasets, original analysis programs and TFL macros as per specific requirements of various country specific reimbursement agencies.Profile:
- Multiple years of relevant clinical trial SAS experience in analysis and reporting. Fast learner.
- 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.
- Team oriented person.
- Capacity to work independently or under the guidance of a senior statistical programmer.
- 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 for this mission.
- 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.
- Language: Able to read, write and speak fluently in English. English writing skills are a must for this mission.
Experience with SAS on PC and UNIX platforms.