Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. Join our exceptional team and embrace a collaborative workspace where personal growth is nurtured, enabling you to make a meaningful global impact. Fortrea is proud to be an Equal Opportunity Employer: As an EOE/AA employer, Fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply. If, as a result of a disability, you require a reasonable accommodation to complete your job application, pre-employment testing, job interview or to otherwise participate in the hiring process, please contact: taaccommodationsrequest@fortrea.com. Please note that this e-mail address is only for job seekers requesting an accommodation. Please do not use this e-mail to check the status of your application.
Senior Statistical Programmer – Sponsor Dedicated
Location
Poland
Posted
142 days ago
Salary
0
Seniority
Senior
Job Description
Senior Statistical Programmer – Sponsor Dedicated
Fortrea
• Review SAPs and TFL shells from a programming perspective. • Advise on the development of complex TFL shells from a programming perspective. • Develop and/or lead the development of complex specifications for SDTMs and ADaM datasets. • Develop and maintain SAS programs to create SDTM and ADaM datasets and TFLs, and perform quality control of SDTM, ADaMs and TFLs. • Produce / define XML / PDFs, Analysis Results Metadata (ARM), aCRFs and Reviewers Guides to support SDTMs and ADaMs. • Respond to QA and client audits and support qualification audits. • Identify and propose innovative ways to improve the efficiency, quality and productivity of our clinical statistical programming business.
Job Requirements
- Degree in a relevant field such as mathematics, life sciences, statistics, computer sciences, etc.
- Solid professional experience as a statistical programmer within a biotech, CRO or pharmaceutical company.
- Demonstrated knowledge of base SAS, SAS macros, SAS/STAT; demonstrated ability to debug SAS programs.
- Proven professional experience with SDTMs, ADaM datasets (safety and efficacy) and TFLs.
- Solid knowledge of CDISC standards.
- Business fluency in English – both spoken and written – is a must.
Benefits
- Flexible work arrangements
- Professional development opportunities
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