Biostatistician / Senior Statistical Programmer I & II

We are the global biostatistics team dedicated to late phase research, working on (but not limited to) peri and post approval research, post authorization safety studies, observational and non interventional studies, patient reported outcomes as well as analyses for abstracts, papers and manuscripts

As a Sr Statistical Programmer II you will be responsible for statistical aspects of clinical and preclinical research projects

Project responsibilities include study design, case report form development, analysis planning and scheduling, analysis and interpretation of data, and reporting of results

May be required to coordinate analysis efforts across multiple research projects conducted for a client

What we need:

Minimum 3 years experience Industry experience in SDTM, ADAM & TLF.

Extensive experience with programming in eg SAS or R

Experience with reporting clinical trials, including statistical data handling, analysis and reporting

Experience with review and documentation of programs

Good knowledge of drug development

Experience with clinical database technologies, data models and advanced programming

Experience with collaboration across professional and regional borders

Regular experience with communication and presentations

In-depth knowledge of computer systems and IT

Good knowledge of GxP and guidelines within drug development

Basic understanding of the pharmaceutical industry and key elements of the value chain, with a focus on immediate stakeholders and how to deliver on own goals

Full time