Principal Statistical Programmer Sponsor Dedicated, EMEA
6 days ago
As a Principal Statistical Programmer in our sponsor-dedicated Flexible Solutions business unit you are central to the successful delivery of complex projects for a renowned innovative and global top pharmaceutical company.You will be involved in liaising with the entire study team as needed including Clinical Medical Writing Safety and Biometrics.It is a great opportunity to see more how this works from a Big Pharma perspective whilst still being part of a global CRO with opportunity for future career growth.This position allows you to participate in the development of innovative new benchmark drugs for a wide variety of therapeutic areas.You can be 100% home-based in EMEA or you can work from our local office in your home country. Your Responsibilities:Plan execute and oversee all programming activities on a study including but not limited to: resource estimation working within budget meeting timelines maximizing quality interaction with other departments etc.Oversee SDTM ADaM and TLF development perform Senior Review of outputs.Liaise with other Sponsor departments for additional programming needs as required to support publications medical writing and additional development needs and analyses.Support/oversee submission activities (especially in late phase team).Ensure all activities are conducted efficiently with appropriate set-up of needed tools and macros prioritizing quality at all times.Mentor less-experienced team members in best practices around SDTMs ADaMs and TFLs while ensuring adherence to department standards and processes.Your Profile:Ideally a degree in a relevant field such as mathematics life sciences statistics computer sciences etc.In lieu of the above: professional experience in statistical programming within clinical trials in a biotech CRO or pharmaceutical company.Solid experience with complex clinical trials (minimum 5 years) and the corresponding data sets content (safety and efficacy) and endpoints.Ideally you will have knowledge in all aspects of clinical trials from initial study set-up to study completion with an understanding of the roles and responsibilities of all related disciplines e.g. Biostatistics and Clinical Data Management.Expert knowledge of base SAS SAS macros SAS/STAT and in debugging SAS programs.Broad knowledge of all CDISC requirements related to SDTM and ADaM including Reviewers Guides and submission standards.An autonomous collaborative work style a curious mind and a keen attention to detail.Fluency in English both verbal and written is a must.Learn more about our EEO & Accommodations request here.Required Experience:Staff IC Key Skills Business Development,Customer Service,Attorney,CISSP,Data Analysis Employment Type : Full-Time Experience: years Vacancy: 1
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Maidenhead, United Kingdom Fortrea Full timeAs a Principal Statistical Programmer in our sponsor-dedicated Flexible Solutions business unit you are central to the successful delivery of complex projects for a renowned innovative and global top pharmaceutical company. You will be involved in liaising with the entire study team as needed including Clinical Medical Writing Safety and Biometrics. It is a...
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Senior or Principal Statistical Programmer
1 week ago
Maidenhead, United Kingdom Fortrea Full timeSenior or Principal Statistical Programmer – OncologyJoin Fortrea as a Senior or Principal Statistical Programmer in our sponsor‑dedicated Flexible Solutions business unit, central to the delivery of complex global oncology clinical trials (Phases I–III) for world‑renowned pharmaceutical companies.As a 100% home‑based role (or office in your home...
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Lead Statistical Programmer
2 weeks ago
Maidenhead, United Kingdom Fortrea Full timeAs a Lead Statistical Programmer in our sponsor-dedicated Flexible Solutions business unit you are central to the successful delivery of complex projects for a renowned innovative and global top pharmaceutical company. You will be involved in liaising with the entire study team as needed including Clinical Medical Writing Safety and is a great opportunity to...
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Lead Statistical Programmer
5 days ago
Maidenhead, United Kingdom Fortrea Full timeAs a Lead Statistical Programmer in our sponsor-dedicated Flexible Solutions business unit you are central to the successful delivery of complex projects for a renowned innovative and global top pharmaceutical company.You will be involved in liaising with the entire study team as needed including Clinical Medical Writing Safety and is a great opportunity to...
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Maidenhead, United Kingdom Fortrea Full timeAs a Senior or Principal Statistical Programmer in our sponsor-dedicated Flexible Solutions business unit you will be central to the successful delivery of complex global oncology clinical trials (Phases IIII) for some of the worlds most renowned and innovative pharmaceutical companies.In this role you will contribute to the development of new and...
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Maidenhead, United Kingdom Fortrea Full timeAs a Senior Statistical Programmer in our sponsor-dedicated Flexible Solutions business unit you are central to the successful delivery of complex clinical trials (phases I-III) for renowned innovative and global top pharmaceutical companies. Oftentimes you will have the opportunity to lead studies through various phases of the clinical development plan and...
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Statistical Programmer II
5 days ago
Maidenhead, United Kingdom Fortrea Full timeAs a Statistical Programmer II in our sponsor-dedicated Flexible Solutions business unit you are central to the successful delivery of complex clinical trials (phases I-III) for renowned innovative and global top pharmaceutical companies. Oftentimes you will have the opportunity to lead studies through various phases of the clinical development plan and...
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Statistical Programmer II
1 day ago
Maidenhead, Berkshire, United Kingdom Fortrea Full timeAs a Statistical Programmer II in our sponsor-dedicated Flexible Solutions business unit, you are central to the successful delivery of complex clinical trials (phases I-III) for renowned, innovative and global top pharmaceutical companies. Oftentimes you will have the opportunity to lead studies through various phases of the clinical development plan and...
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Statistical Programmer II
2 weeks ago
Maidenhead, United Kingdom Fortrea Full timeYour Responsibilities With sufficient experience assume the role of a Lead Statistical Programmer for CP studies only with support from senior programming staff. Plan execute and oversee all programming activities on a study including but not limited to resource estimation working within budget meeting timelines maximizing quality interaction with other...
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Senior or Principal Statistical Programmer
1 week ago
Maidenhead, Windsor and Maidenhead, United Kingdom Fortrea Full time £60,000 - £90,000 per yearAs a Senior or Principal Statistical Programmer in our sponsor-dedicated Flexible Solutions business unit, you will be central to the successful delivery of complex global oncology clinical trials (Phases I–III) for some of the world's most renowned and innovative pharmaceutical companies.In this role, you will contribute to the development of new and...
