Clinical SAS Programming Made Easy

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SAS Programming Made Easy

Technology-driven SAS Professional and Senior Statistical Programmer with over 6 years’ experience in Pharmaceutical and Biotech environments.

Work closely with Statisticians and programming team member’s on Clinical Trial Studies for NDA submissions.

Exemplary analytical and documentation abilities with extensive experience in Engineering, Government and Clinical Studies.

Experience in SAS in all Phases of the clinical trial process. Articulate, Commutative and an excellent leader.

Applies well-honed talents in strategic problem solving, cost-savings objectives, and long-range goals.

Qualifications include:

Specialized expertise in SAS programming and Statistical Programming.

Lead Programmer, in Multiple Phase studies, Neurology, Oncology, Toxicology, Infectious Diseases.

Articulate, innovative, and able to perform proficiently in a high-energy, fast-paced environment.

Identify and resolve differences with table programmers.

QC programmer of more than 180 summary tables and listings.

Conduct code reviews.

Broad technical background driving the development of information and database systems to optimize the use of existing infrastructure, maximize individual productivity, and help the company reach its full potential.

Substantially reduced code in current patient profile program to speed up compile time process and make code more readable.

Spearheaded the development of SAS programs using SAS graph to produce bar charts, scatter plots and pie charts of scorpion anti-venom.

Instrumental in the FDA market acceptance of a new drug by performing the development and implementation of the analytical datasets used for NDA submissions.

Successfully developed and implemented an accurate, effective and systematic process to dramatically improve manufacturing processes.

Effectively analyzed pre-clinical data for the preparation of 15 toxicology studies and analyzed One-way analysis of variance, Nested analysis of variance and trend analysis.