Fortrea
Fortrea is a clinical research organization (CRO) with over 30 years of experience dedicated to accelerating the development of life-changing treatments by providing comprehensive clinical solutions for biopharma and MedTech companies. They offer a range of services including clinical trial management, pharmacology services, and regulatory strategy, all designed around the needs of their clients. Fortrea's mission is to put patients at the center of their work, aiming to bring innovative therapies to market faster through tailored, data-driven approaches.
clinical research • clinical trials
10,000+ employees
💊 Pharmaceuticals
Lead Statistical Programmer - SAS
January 6
Fortrea
Fortrea is a clinical research organization (CRO) with over 30 years of experience dedicated to accelerating the development of life-changing treatments by providing comprehensive clinical solutions for biopharma and MedTech companies. They offer a range of services including clinical trial management, pharmacology services, and regulatory strategy, all designed around the needs of their clients. Fortrea's mission is to put patients at the center of their work, aiming to bring innovative therapies to market faster through tailored, data-driven approaches.
clinical research • clinical trials
10,000+ employees
💊 Pharmaceuticals
📋 Description
• Plan, execute and oversee all programming activities on a study • Oversee SDTM, ADaM and TLF development • Liaise with other Sponsor departments for additional programming needs • Support/oversee submission activities • Ensure all activities are conducted efficiently • Mentor less-experienced team members
🎯 Requirements
• Ideally, a degree in a relevant field such as mathematics, life sciences, statistics, computer sciences, etc. • Professional experience in statistical programming within clinical trials in a biotech, CRO or pharmaceutical company • Solid experience with complex clinical trials (minimum 5 years) • Previous Lead experience preferred • Knowledge in all aspects of clinical trials, from initial study set-up to study completion • Expert knowledge of base SAS, SAS macros, SAS/STAT and debugging SAS programs • Broad knowledge of all CDISC requirements related to SDTM and ADaM • An autonomous, collaborative work style, a curious mind and keen attention to detail • Fluency in English – both verbal and written – is a must
🏖️ Benefits
• Equal Opportunity Employer • Diversity and inclusion in the workforce • Commitment to personal growth
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