Principal Analyst, Clinical Programming - CNS (Central Nervous System)
Principal Analyst, Clinical Programming - CNS (Central Nervous System)
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Salary Not Disclosed
1 Vacancy
Job Description
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 require must have 6 years:
- performing in statistical programming in the CRO or Pharmaceutical Industry;
- applying SAS programming concepts across SAS/Base SAS/STAT SAS/Graph SAS/IML & SAS/SQL; &
- 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
Additional Information :
Salary Range: Salary Range: $164609.51 - $178500.00 per year
Apply online at or send resume to . Refer to Req ID: REF43611U
We offer a comprehensive package of benefits including paid time off (vacation holidays sick) medical/dental/vision insurance and 401(k) to eligible employees. This job is eligible to participate in our short-term and long-term incentive programs.
AbbVie is committed to operating with integrity driving innovation transforming lives serving our community and embracing diversity and inclusion. It is AbbVies policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race color religion national origin age sex (including pregnancy) physical or mental disability medical condition genetic information gender identity or expression sexual orientation marital status status as a protected veteran or any other legally protected group status.
AbbVie is an equal opportunity employer and is committed to operating with integrity driving innovation transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more visit & Puerto Rico applicants seeking a reasonable accommodation click here to learn more:
No
Employment Type :
Full-time
Employment Type
Full-time
