Senior Principal Statistical Programmer, SAS Viya, R, Python

🕒 il y a 2 mois

🇬🇧 Royaume-Uni – Télétravail

⏰ Temps Plein

🟠 Senior

🔙 Ingénieur Back-end

🇬🇧 Parrain de Visa de Travailleur Qualifié UK

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👻 Score fantôme 32%

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🗣️🇺🇸🇬🇧 Anglais requis

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Logo of Syneos Health

Syneos Health

10 000+ employés

🏥 Santé

💼 Conseil

📦 Logistique

Healthcare • Consulting • Logistics

Syneos Health est une organisation de solutions biopharmaceutiques entièrement intégrée et leader, conçue pour accélérer le succès des clients. Ils transforment des intuitions cliniques, des affaires médicales et commerciales uniques en résultats pour répondre aux réalités du marché moderne. En utilisant des technologies avancées et des perspectives, Syneos Health collabore avec les clients pour accélérer la livraison de thérapies importantes aux patients dans le monde entier, offrant des services qui couvrent tout le spectre du clinique au commercial.

Description

• Migration support to SAS Viya • Analyzes information and develops innovative solutions to programming and data analysis challenges across the department. • Develop or review specifications and may support any kind of statistical programming activity. • Displays willingness to work with others, holds project team members accountable, and leads projects and initiatives as necessary to meet the needs of the business.

🎯 Exigences

• Provides statistical programming technical support and expertise across the Biostatistics function and other departments as needed. • Uses SAS or other software to develop custom programming code to generate summary tables, data listings, graphs and derived datasets as specified in the statistical analysis plan and programming specifications. • Proposes and leads the development of process improvements, programming tools and macros for standardization and efficiency, and the development of new concepts, technologies and products to meet emerging customer needs. • Analyzes information and develops innovative solutions to programming and data analysis challenges across the department. • Reviews, provides input, and promotes standardization of CRFs, databases, Statistical Analysis Plans and mock shells within a project or therapeutic area, or across a program. • Mentors other members of the Biometrics Department in the use of traditional, new, and novel approaches in delivering analytics to sponsors and regulatory agencies through the development and presentation of training courses and one on one discussion. • Understands and enforces compliance with company, regulatory, and industry standards, within and across projects or programs. • Maintains well organized, complete, and up-to-date project documentation, testing, and verification/quality control documents and programs ensuring inspection readiness. • Maintains extensive working knowledge of clinical drug development, industry standards, and electronic submission requirements.

🏖️ Avantages

• We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program. • We are committed to building an inclusive culture – where you can authentically be yourself.

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