Senior Programmer - SAS, Switzerland

For our Life Sciences client in Switzerland, we are urgently seeking for a Senior Programmer with experience and interest in defining and implementing a computing environment will support a Pharma Development initiative to deploy a future data analytics platform.

Job title: Senior Programmer
Start date: ASAP
End date: 31/10/2017
Location: Basel, Switzerland
Language: English

Your role:

- Responsible for the integrity of the programming/computing solutions for multiple clinical trials (or equivalent).
- Is the scientific lead for programming expertise liaising with Biometrician and statistical scientific counterparts within the team, across multiple clinical trials
- Leads the full execution of final production output generation (tables, listings and graphics) for clinical trials. May lead programming activities for a relatively small project or an indication with guidance.
- In conjunction with the Biometrician/Statistical Scientist, develop study-level programming standards and ensure compliance with project-level/company standards. With guidance, may provide support to development of project-level programming standards, following internal guidelines.
- Ensure that documents and specifications are consistent and comply with company standards by providing input into eCRF and data structures, tables, listings and figures for Phase I-IV clinical trials and submission activities.
- Responsible for programming (according to specifications) analysis datasets, pooled datasets, listings, tables, and figures for Phase I-IV clinical trials and for SCS and SCE with high quality and within milestones.
- Responsible for preparing Case Report Tabulations for the submission as required.

Your experience:

- Education ; BA/BS/MS equivalent experience in mathematics, statistics, computer science, or health sciences/related field.
- At least 4 years work experience in a programming role preferably supporting clinical trials/or in the pharmaceutical industry (2 years for MS Statistics/Computer Science graduates).
- Intermediate knowledge of/experience with SAS and other relevant programming software.
- Working knowledge of database design/structures and basic statistics.
- Good understanding of global clinical trial practices, procedures, methodologies.
- Good understanding of regulatory requirements relevant to statistical programming (eg GCP, ICH).
- Excellent knowledge of data architecture

We welcome applications of consultants' who match most of the above requirements and are available on a short notice. There is a competitive Hourly rate available for the contract; alternative market rates are also welcome.

We hope that the role will be of interest to you and understand that further information may be required prior to an application to the end client, please feel free to email or call me at anytime with any questions you may have.

Thank you for your time and we hope to hear from you soon.

Kind regards,

Neha Sharma
Pharmaceutical & Life Sciences Business Developer
Recruiting Team MBA,
Michael Bailey Associates

Michael Bailey International is acting as an Employment Business in relation to this vacancy.