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Position Overview
As a Senior Statistical Programmer, 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. This role can be performed as fully remote.
Our values
* We believe in applying scientific rigor to reveal the full promise inherent in data.
* We nurture intellectual curiosity and encourage everyone to approach new challenges with enthusiasm and the desire for discovery.
* We believe in collaboration and invite a diversity of perspectives, drawing on a variety of talents to create a wealth of possibilities.
* We prize innovation and seek intelligent solutions using leading-edge technology.
How You Will Contribute
* Perform data manipulation, analysis and reporting of clinical trial data, both safety and efficacy (ISS/ISE), utilizing SAS programming.
* Generate and validate SDTM and ADaM datasets/analysis files, and tables, listings, and figures (TLFs).
* Produce and QC/validate programming.
* Generate complex ad-hoc reports utilizing raw data.
* Apply strong understanding of efficacy analysis.
* Create and review submission documents and eCRTs.
* Communicate with and/or respond to internal cross-functional teams and clients for project specifications, status, issues or inquiries.
* Perform lead duties when called upon.
* Serve as a team player, with a willingness to go the extra distance to get results, meet deadlines, etc.
* Be adaptable and flexible when priorities change.
Qualifications
* Bachelor's degree in Statistics, Computer Science, Mathematics or related field.
* At least 8 years of SAS programming experience with clinical trial data in the pharmaceutical & biotech industry; a bachelor's degree is required, at least 6 years of related experience with a master's degree or above.
* Study lead experience, preferably juggling multiple projects simultaneously.
* Strong SAS data manipulation, analysis and reporting skills.
* Solid experience implementing the latest CDISC SDTM / ADaM standards.
* Strong QC / validation skills.
* Good ad-hoc reporting skills.
* Proficiency in efficacy analysis.
* Familiarity with drug development life cycle and experience with the manipulation, analysis and reporting of clinical trials data.
* Submissions experience utilizing define.xml and other submission documents.
* Experience supporting immunology, respiratory or oncology studies is a plus.
* Excellent analytical & troubleshooting skills.
* Ability to deliver quality output in adherence to challenging timelines.
* Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners.
Seniority level: Mid-Senior level
Employment type: Full-time
Job function: Information Technology
Industries: Software Development
Cytel Inc. is an Equal Employment / Affinitive Action Employer. Applicants are considered for all positions without regard to race, color, religion, sex, national origin, age, veteran status, disability, sexual orientation, gender identity or expression, or any other characteristics protected by law.
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