Senior SAS Programmer
Vifor Pharma
Zurich, Glattbrugg,Switzerland
vor 6 Tg.

About You

We are currently looking for a Senior SAS programmer. Reporting directly to the Global Head of Biometrics, you will provide support to all Vifor Pharma clinical studies and statistical projects.

Within this function, you will :

Act as the SAS programmer representative in clinical study and project teams and provide SAS programming expertise

Coordinate and monitor outsourced SAS programming activities

Review and approve the SAS programming deliverables, including programming of SDTM, ADaM and outputs production, and the preparation of the technical documents (specifications)

Ensure that quality control is performed on all programs, and that the outputs meet quality standards and project requirements

Lead the development and the update of the biometrics standards and SOPs

Coordinate and contribute to the preparation of the FDA and EMA submission filing or responses to the health authorities

Participate in the preparation of the integrated analyses of safety and efficacy (ISE / ISS)

Provide strategical input to and lead SAS programming activities

Prepare, plan and run SAS programming activities according to the projects timelines

Manage all technical documentation such as SDTM, ADaM, good programming practices, and Open CDISC validation reports associated to the development of SAS programs across all SAS programming activities.

YOUR PROFILE :

The successful candidate holds a University level degree (BSc or higher level) in health related field and / or computational science (Degree in Biology or biostatistics would be an advantage) and brings additionally the following knowledge and experience :

3 to 5 years of statistical programming experience in clinical trials

3 to 5 years of SAS programming experience, using SAS BASE, STAT, MACRO and GRAPH

Demonstrated and applied experience in the use of CDISC standards (SDTM and ADaM)

Good knowledge of GCPs, including local laws, ICH and other regulatory guidelines (in particular eCFR part 11 compliant)

Basic or advance knowledge of statistical principles and methods

Experience managing CROs and experience in the technical validation and installation of SAS or other programming tools are an asset

Abilities to develop, update and / or maintain complex SAS macros

Fluent English both written and spoken

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