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2 days ago
This is a sponsor-dedicated position where you will work fully embedded within one of our pharmaceutical clients, with the support of Cytel behind you.
You will leverage your advanced SAS programming skills and proficiency in CDISC standards (SDTM & ADaM) to support or lead one or more Phase I-IV clinical trials.
- As a Senior Statistical Programmer, you will apply scientific rigor to reveal the full promise inherent in data.
- Collaboration and intellectual curiosity are key to success in this role. We invite diverse perspectives and talents to create possibilities.
- Our approach emphasizes innovation and seeking intelligent solutions using leading-edge technology.
Contribute by:
- Performing data manipulation, analysis, and reporting of clinical trial data, both safety and efficacy (ISS/ISE), utilizing SAS programming
- Generating and validating SDTM and ADaM datasets/analysis files, and tables, listings, and figures (TLFs)
- Production and QC/validation programming
- Generating complex ad-hoc reports utilizing raw data
- Applying strong understanding/experience of Efficacy analysis
- Creating and reviewing submission documents and eCRTs
- Communicating with and/or responding to internal cross-functional teams and client for project specifications, status, issues, or inquiries
- Performing lead duties when called upon
- Serving as a team player, with a willingness to go the extra distance to get results, meet deadlines, etc.
- Being adaptable and flexible when priorities change
Enjoy a dynamic work environment that supports collaboration, innovation, and professional growth.
- Develop your technical expertise through continuous learning opportunities
- Contribute to high-profile projects with a global impact
- Grow your career in a supportive company culture
We pride ourselves on fostering a culture that values diversity, inclusivity, and creativity. Join us in shaping the future of biopharmaceutical research and development.
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