Cpl Life Sciences

Principal Statistical Programming Lead

Location
Central London / West End
Posted
12 Jun 2021
Closes
12 Jul 2021
Ref
JO-2105-468131
Contact
Stephen Wincott
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)

Principal Statistical Programming Lead

Location: Fully Remote working offered

Salary: Highly competitive salary, car allowance, bonus and benefits package

We are partnering exclusively with a large Pharma who are looking for a pivotal hire as the Principal Statistical Programming Lead who will be responsible for advancing the statistical programming methods and capabilities in highly complex, global projects to ensure they lead the way in analysis and reporting.

We need an individual who can bring specialist scientific, technical, and problem-solving skills to take a lead role, share knowledge, develop team members and deliver highly sophisticated clinical projects. In return, our Client is offering a market leading salary & benefits package with full remote working.

A highly visible role, the Statistical Programming Lead will be working on multiple clinical projects and will plan, coordinate and deliver the teams activities whilst providing technical and project specific guidance to ensure quality and results. Responsible for adoption of new processes & technology on assigned projects/programs in collaboration with Technical groups and statistical programming portfolio leads. Responsible for adoption of new processes & technology on assigned projects/programs in collaboration with Technical groups and statistical programming portfolio leads.

You will develop the programming strategy for one or more clinical projects and will review and have input into the project requirements and documentation. You will apply your technical expertise to develop and implement solutions on projects to increase efficiency using cutting edge tools and methodologies.

You will have a minimum of a BSc or higher in statistics, computer science, mathematics, data science/analytics or related scientific field experience. Advanced degree (Masters, PhD or equivalent) preferred.
Advanced knowledge of statistical programming languages such as SAS, R, R-Shiny or Python. A strong communicator, able to coordinate programming activities and leading teams. Sophisticated knowledge of industry standard data structures, detailed understanding of end to end clinical trial process and relevant clinical research concepts
Demonstrated experience planning and coordinating complex programming strategy and activities with the ability to support multiple high complexity tasks.
Demonstrated experience leading programming teams to meet project timelines and goals.

Interested, please send your CV to Stephen Wincott at stephen.wincott@cpl.com

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