Synta Pharamceutical Opportunities

From sasCommunity

Sr. SAS Programmer

Synta Pharmaceuticals is seeking an experienced Sr. SAS programmer to contribute to the success of the programming team through delivery of high quality and timely deliverables. The programmer will develop and maintain general-purpose and ad hoc SAS programs for the analysis and reporting of clinical and/or post marketing data, perform QC task to ensure accuracy, and participate in functional process and technology initiatives.

Responsibilities:

• Provide general SAS programming support to Clinical Research and Development.

• Work closely with statisticians to generate analysis data sets and create tables, listings and graphs for interim analyses, preliminary reports and Clinical Study Reports for in-house use, publications, and/or regulatory submissions.

• Perform quality control checks on program code and outputs produced by other team members.

• Conduct data edit checks to ensure the quality of source data.

• Enhance existing utility programs and develop new utility macros to standardize data processing and output procedure.

• Review and provide input on programming related documentation including plans and specifications.

• Manage programming timelines, schedules, and activities on specific programming tasks.

• Report to Associate Director of Statistical Programming.

Qualifications:

• Bachelor’s degree in life science, statistics, mathematics, computer science, or related field required; Master’s degree preferred.

• 5+ years of SAS programming experience in biotech or pharmaceutical industry.

• Experience in SAS programming language, macros, and procedures.

• Working knowledge of ISS/ISE, CDISC standards (SDTM, ADaM).

• Detail oriented, and strong organizational and communication skills.

• Ability to work in a team environment.

Please visit [1] to apply for this opportunity

Location: Lexington, MA