Senior – Principle Programmer Analyst– World leading Pharma – $100 - $135k + Benefits

Senior – Principle Programmer Analyst– World leading Pharma, Top Ten Globally – $100 - $135k + Benefits – King of Prussia, Pennsylvania

Suitable for: SAS Programmer, Statistical Programmer, SAS Analyst, Senior SAS Programmer, Principal Statistical Programmer, Principal SAS Analyst

Company Background:

One of the world's leading pharmaceutical companies, with statisticians and programmers working across worldwide sites. In recognition of the developing sophistication and technical requirements of the programming role, the Clinical Programming department was formed as a standalone department within the broader Clinical Statistics group over 1 year ago, covering all phases of drug development in a wide range of therapeutic areas.

Please Contact Emily O’Brien on 646-569-9081 or email Emily.obrien@peoplewithchemistry.com if you would like to know more about this opportunity. This will be 100% confidential.

Position Summary:

In addition to the group’s activities supporting the pipeline of drugs, key accountabilities may include developing and implementing strategies for programming resourcing using both internal, external, onshore and offshore resource; driving CDISC implementation for the reporting of clinical trials; and identifying and implementing IT solutions to offer further benefit and efficiency for the group’s activities.

Responsibilities:

  • Plan and manage programming activities across multiple studies, asset(s), indication or function to deliver all data analysis outputs to agreed timelines and quality.
  • Oversee outsourced tasks to third party vendors and ensure their performance meets the agreed timelines, quality and budget requirements established for the project or study.
  • Define, develop and embed standards within a function, or therapeutic area in accordance with industry standards
  • Responsible for programming and QC across a study/asset including submission activities.
  • Review and input into key documents at the project level (e.g. submission documents, clinical reports and publications). May author or co-author reporting analysis plans and department level documents (e.g. SOPs, working practice document).
  • Participate in the design of other study delivery components (e.g. case report forms, study databases).
  • Provide tools that add value at study team and functional team level
  • Act as key statistical programming contact for internal and external business partners.
  • Provide broader technical knowledge and expertise (e.g. UNIX scripting, computing environments). Provide technical advice to other teams and departments.
  • Provide oversight, training and performance feedback to less senior programmers.

Please Contact Emily O’Brien on 646-569-9081 or email Emily.obrien@peoplewithchemistry.com if you would like to know more about this opportunity. This will be 100% confidential.

Keywords: CDISC, SAS, Statistical, Programming, Programmer, Analytical, Analyst, Statistics, Clinical Trails, Studies, Drug Development

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