Statistical Programmer
Statistical Programmer
Your Role
As a Senior Statistical Programmer, you will:
- Develop and execute statistical programming tasks for internal and external purposes, including health authority interactions, such as briefing books and conference presentations.
- Provide oversight of CRO statistical programming activities, ensuring quality and adherence to timelines.
- Produce statistical outputs according to specifications for internal data reviews and clinical trial updates.
- Review SDTM and ADaM specifications and datasets, contributing to the development of internal specifications for analysis datasets.
- Program and update dashboards for ongoing studies, ensuring accurate and timely information flow.
- Engage in project management of programming activities across multiple trials, enhancing the efficiency and output of our biometrics functions.
Your Profile
We are looking for a candidate with:
- A University Degree in Science or a related field; an advanced degree is preferred.
- At least 5 years of experience in the pharmaceutical industry with a solid foundation in statistical programming.
- Proficiency in SAS, R, and familiarity with CDISC standards, including specific knowledge of RECIST 1.1.
- Demonstrated ability to work collaboratively across various teams, including Biostatistics, Clinical Data Management, Pharmacovigilance, and Clinical Operations.
- A proactive approach to risk management, with a track record of delivering high-quality clinical data on time and within budget.
This role is designed for a detail-oriented professional who excels in a dynamic environment and is eager to take on challenges in clinical trial programming. If you are driven by quality, efficiency, and the opportunity to advance cutting-edge pharmaceutical research, we encourage you to apply and join our team in pushing the boundaries of medicine.
Why Merus?
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