Sr. Statistical Programmer (DG)
Job Location: Parsippany, NJ (see all jobs in NJ)
Work Type: Remote
Date Posted: 2022-03-02
Works collaboratively with Clinical Development staff to meet project deliverables and timelines for statistical data analysis and reporting. Assesses the quality and consistency of analysis data and performs cross-study analyses. Uses internal macros or writes SAS® macros to automate study deliverables. Works as a primary programmer for multiple Phase 1-4 studies. Assists in submissions of electronic data (e.g., SAS® data sets) to regulatory agencies. Independently develops analysis specification & programs. Identifies potential issues in study documentation and proposes solutions. Contributes to strategic initiatives. Assist with study and systems audits by Compliance Group and external bodies, and respond to audit questions and findings. Promote and communicate awareness of programming and the role of the Biometrics department (internal/external; scientific/process). Excellent verbal and written communication skills and interpersonal skills are required. Has thorough knowledge of clinical trial study design and electronic data submission requirements. Must be able to work independently on multiple concurrent projects.
2 years of experience and a MS degree in Biostatistics/Computer Science or equivalent. 1-2 years SAS/Statistical Programming experience.
Please contact Darren Gutowski at firstname.lastname@example.org
Base up to 120k+bonus+stock
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