Aktualne oferty pracy związane z Senior Clinical Programmer Lead - Warszawa, Mazovia - IQVIA Argentina
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Senior Clinical Programmer
3 tygodni temu
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Senior Clinical Programmer
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Senior Clinical Project Lead
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Clinical Operations Lead
1 dzień temu
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Clinical Operations Lead
1 tydzień temu
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Lead/Senior Gameplay Programmer
1 tydzień temu
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Clinical Documentation Lead
2 dni temu
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Senior Engine Programmer
3 tygodni temu
Warszawa, Mazovia, Polska Mapcore Pełny etatThe Senior Engine Programmer will be responsible for designing, implementing, optimizing and maintaining parts of our in-house engine both for the PC and the new generation of consoles (PS4, Xbox One). He/she needs to cooperate with other engine programmers and the Lead Engine Programmer in order to create technical solutions meeting desired...
Senior Clinical Programmer Lead
2 tygodni temu
As a Senior Clinical Programmer at IQVIA, you will lead the development and maintenance of data quality standards and perform the necessary programming and validation steps to ensure that regular and on-demand data quality control can be performed in clinical studies. This role will support the clinical study team with the identification, specification, and implementation of relevant listings and reports to ensure that adequate data quality will be achieved for clinical trials.
This includes collaborating with the clinical study team in developing ongoing data quality standards and clinical data acceptance rules for clinical data in the eCRF and related external data sources collecting data from clinical studies. The successful candidate will also lead the implementation and maintenance of internal data quality control programs, acceptance criteria for data from external sources, and performs the related programming.
You will work effectively in a team setting, and to meet set goals by managing your own timelines. You will also collaborate with peers, data management, and statistics to ensure the quality and accuracy – thus submission readiness – of clinical data as required by authorities (i.e., SDTM, ADaM, define.xml). Supports the review of related deliverables.
The ideal candidate will have a degree in Computer Science, Mathematics/Statistics, or a related area with relevant experience. At least 5 years of experience in either clinical data management and/or statistical programming within the CRO/pharmaceutical environment is required. Understanding of data management and/or statistical programming processes and standards, knowledge in CDISC standards (CDASH, SDTM, ADaM), and ability to work in cross-functional, multicultural, and international clinical trial teams are essential.
