10.000+
Jobs in Swansea, Gran Bretaña
Principal Statistical Programmer - Sponsor Dedicated
Fortrea
Thatcham
A distancia
GBP 60.000 - 90.000
Hoy
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GBP 70.000 - 80.000
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GBP 60.000 - 80.000
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Gran Bretaña
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A distancia
GBP 26.000 - 40.000
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A distancia
GBP 55.000 - 75.000
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Principal Statistical Programmer - Sponsor Dedicated
Fortrea
Thatcham
A distancia
GBP 60.000 - 90.000
Jornada completa
Hoy
Sé de los primeros/as/es en solicitar esta vacante
Descripción de la vacante
A global pharmaceutical company is seeking a Principal Statistical Programmer to oversee programming activities for complex clinical trials. You will work collaboratively with various departments while mentoring junior team members. The ideal candidate has over 5 years of experience in statistical programming and fluency in English. This position offers the flexibility to be home-based or to work from a local office.
Formación
- Professional experience in statistical programming within clinical trials is essential.
- Minimum of 5 years of experience with complex clinical trials.
- Fluency in English, both verbal and written.
Responsabilidades
- Plan, execute and oversee programming activities on studies.
- Oversee the development of SDTM, ADaM, and TLFs.
- Mentor less-experienced team members.
Conocimientos
Statistical programming
Knowledge of CDISC requirements
SAS programming
Mentorship
Collaboration
Attention to detail
Educación
Degree in mathematics, life sciences, statistics, or computer sciences
Herramientas
SAS
SAS macros
Descripción del empleo
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:
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.
- 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 define.xml, Reviewer's 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.
* El índice de referencia salarialse calcula en base a los salarios que ofrecen los líderes de mercado en los correspondientes sectores. Su función es guiar a los miembros Prémium a la hora de evaluar las distintas ofertas disponibles y de negociar el sueldo. El índice de referencia no es el salario indicado directamente por la empresa en particular, que podría ser muy superior o inferior.
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