Contract Statistical Programmer

Job Description

Key Responsibilities & Requirements:

• Proven background in Oncology studies
• Comfortable with a blend of hands-on programming and study lead responsibilities
• Strong knowledge of CDISC standards (SDTM, ADaM)
• Proficient in SAS, SQL, STAT, Graph
• Experience with SAPs and process development/improvement
• Exposure across phases I–IV and generating TLFs
• Ability to work independently and drive timelines
• Previous experience within CRO or pharmaceutical environments

This is a great opportunity to work on high-impact studies in a collaborative environment with a respected name in the industry.

Are you interested in this position?

Apply by clicking on the “Apply Now” button below!

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