Recruiting biostatisticians in Sweden
Responsibilities and tasks
Biostatisticians will be heavily involved in clinical study design discussions, clinical protocols and Statistical Analysis Plan (SAP) development, preparing data standard specifications (ADAM), conduct statistical programming (using SAS and R), performing statistical analyses, documentation of the results as well as discussing interpretation with customers. Tasks also include internal process development and business development activities.
The biostatistician work in close collaboration with 4Pharma’s statistical programmers, clinical data managers and medical writers as well as the clinical/medical teams at our customers both local and global.
Our office is based in Lund in Sweden and you will be part of our experienced Nordic statistics team. Exact role and title will be discussed based on your profile and preference.
You have solid experience of SAS programming and a good understanding of clinical databases and CDISC data standards.
Excellent skills in both written and spoken English is a requirement. As a person, you are thorough, happy to take on responsibilities, proactive, flexible and enjoy working in a team. You are focused on quality and always have customer perspective on the top of your mind.
What we offer
We look forward to hearing from you!
Please send your CV and cover letter to email@example.com by December 31. We will review candidates as they come in.