Principal/Senior Statistical Programmer
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Job Description
Experienced Statistical Programmer leading programming activities for bioforum's clinical trials. Collaborate in a team to deliver high-quality statistical outputs and ensure compliance with regulatory standards.
Responsibilities:
- Lead statistical programming teams to deliver on projects and communicate directly with the sponsor.
- Oversee and/or be responsible for the quality and validation of statistical output produced.
- Create or review SDTM and/or ADaM dataset specifications.
- Program and/or validate SDTM and ADaM datasets, and TLFs.
- Provide guidance and input on the statistical programmer requirements and queries during the conduct of the trial.
Requirements:
- B.Sc degree in Life / Computer Science, Statistics, or equivalent.
- Minimum 5 years’ experience working as a Statistical Programmer.
- Experience leading a team will be an advantage.
- In-depth knowledge of either CDISC SDTM and/or ADaM standards.
- Advanced knowledge of SAS, including SAS Macros.
- Proven ability to program medium- to high complexity statistical output.
- Excellent communication skills.
- Prior oncology experience and/or team leadership experience is advantageous.
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