Principal Analyst, Clinical Programming - CNS (Central Nervous System)

Statistical Programmer

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas immunology, oncology, neuroscience, and eye care and products and services in our Allergan Aesthetics portfolio.

Key Responsibilities:

• Work independently in executing statistical programming tasks and delivering high quality, timely results.
• Develop & oversee development of Statistical Analysis System (SAS) programs for creation of Analysis Data Model (ADaM) data sets following Clinical Data Interchange Standards Consortium (CDISC) standards.
• Support integrated summaries (ISE/ISS), CSR, conferences/publications, ad-hoc analyses and regulatory deliverables.
• Contribute to the development of standards / best practices within the Statistical Programming functional area that are consistent with highest industry standards.
• Build strong collaborations with Statistics, Data Sciences, Medical Writing, Regulatory Publishing & Clinical Operations.

Qualifications:

Education & Experience:

Must have a BS or foreign educational equivalent in Statistics, Biostatistics, Computer Science, Mathematics or related Scientific area, & 6 years of SAS Programming experience in clinical trials.

Of the experience required, must have 6 years:

1. performing in statistical programming in the CRO or Pharmaceutical Industry;
2. applying SAS programming concepts across SAS/Base, SAS/STAT, SAS/Graph, SAS/IML, & SAS/SQL; &
3. developing SAS programs for the creation of ADaM data sets following CDISC standards, & for the creation of Tables, Listing, & Figures.

Of experience required, must have 3 years of clinical trial programming experience in CNS.

Of experience required, must have 2 years working in a matrixed organization preparing written & oral presentations for peers, business & scientific stakeholders.

Alternatively, would accept a MS/MA or foreign educational equivalent in Statistics, Biostatistics, Computer Science, Mathematics or related Scientific area, & 3 years of SAS Programming experience in clinical trials.

Of experience required, must have 3 years of (i), (ii), (iii) & 1 year working in a matrixed organization preparing written & oral presentations for peers, business & scientific stakeholders.

Of experience required, must 2 years of clinical trial programming experience in CNS.

With either alternative, must have experience preparing clinical data for at least 1 FDA Advisory Committee meeting.

Work experience may be gained concurrently. Will accept any reasonable combination of education, training & work experience.

100% Telecommuting permitted

Salary Range: $164,609.51 - $178,500.00 per year

Apply online at https://careers.abbvie.com/en or send resume to Job.opportunity.abbvie@abbvie.com. Refer to Req ID: REF43611U