Job Description

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Summary:

• This role is a hands on statistical programmer supporting study and asset teams in the delivery of less complex statistical programming deliverables
• Ensures excellence in the programming of analysis ready datasets, tables, listings, and figures, and qc work for which they are responsible
• Ensures adherence to high quality programming standards in their daily work.

Responsibilities:

• Accountable for their assigned work in the programming space supporting the programming leads for a particular study or asset deliverable
• Ensures appropriate documentation and QC documentation for their deliverables
• May provide supportive QC work for other programmers deliverables
• Works with programming leads to ensure clear specifications for their programmed deliverables are in place.
• Will be learning in the space of programming and data standards

Experience Skills:

• Bachelor or Master (preferred) Degree in Statistics, Biological Sciences, IT, or related field.
• At least 1-2 year relevant experience in SAS programming and knowledge of clinical trials
• Statistical Programming and SAS handon experience
• Working knowledge of clinical data
• Strong written and oral communication skills, and time management skills
• Proven ability to manage timelines
• CDISC experience desirable.

Skills Required: Time Management Skills,Medical Knowledge,Clinical Data Management,Biotechnology,Statistical Programming,SAS Programming,Clinical Trials,Bio-Statistician