Job Description

Responsibilities:

Create or review and approve programming plans at study and project level.

Provide input on key study-related documents produced by other functions (e.g. CRFs, Data Management Plan, SAPs, etc.)

Create or review and approve CDISC-compliant datasets and corresponding documentation for electronic submission to regulatory agencies.

Develop software systems to generate displays of clinical study data as tables, listings, and graphs for electronic submission to regulatory agencies.

Assist statisticians by suggesting algorithms to address Client analysis requests.

Develop software validation procedures and test plans, as necessary.

Create and document archives of software, outputs, and analysis files.

Create and maintain department SOPs related to clinical programming.

Requirements:

Bachelor's degree in computer science, Statistics, Mathematics, Life Sciences, or other relevant scientific fields; master's degree preferred.

Minimum of 5years of experience in developing software for clinical trials using the SAS system

Skilled in programming with SAS. Knowledge of additional programming languages a plus.

Good knowledge of statistics and drug development process

Experience as a lead programmer for NDAs/BLAs

Experience overseeing the work of internal contractors and external vendors (CROs)

Experience in pharmacokinetics/pharmacodynamics modeling a plus.

Familiarity with CDISC standards, including SDTM and Adam models.

Solid verbal and written communication skills

Job Tags

Permanent employment, For contractors,

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