Biostatistician and SAS Programmer

Datum:  2-okt-2022
Categorie:  Clinical & Medical

Bij Terumo verbeteren we levensreddende medische technologieën voor onze samenleving. 
Gretig om ook bij te dragen aan de gezondheid van mensen en het welzijn van patiënten? We dagen je uit om een meester te worden in jouw vakgebied. Investeer je talenten in balans met je persoonlijke ambities. Leven en werken in harmonie. 
Vanuit onze Japanse oorsprong, worden we gedreven door respect, eigenaarschap en voortdurende verbetering. 
Het is de kern van alles wat we doen. Zo maken we een verschil in het leven van patiënten, klanten en medewerkers.

Department Info

 

The objectives of the European Medical and Clinical Division (EMCD) are to organize, manage and conduct clinical trials by respecting all regulatory requirements and Good Clinical Practice, to communicate clinical data to wider audience, to manager all medical aspects of company products, and to contribute to the new products and new therapies development. 

Job Summary

 

As Biostatistician and SAS programmer, you report to the EMEA Biostatistics Manager. You collaborate with the clinical & medical team to analyse our clinical studies, prepare for publications or make customised presentations for congresses, and support design of Investigator initiated Trials. 

Job Responsibilities

 

1.    Implementation of statistical analysis
⦁    Responsible for development of statistical analysis plan, including mock table shells
⦁    Responsible for SAS programming of ADaM and TFL for all studies conducted in EMCD
⦁    Analyse, interpret data and report conclusions to different target audiences.
⦁    Support development of statistical and analytical innovative methods such as data visualisation, machine learning, deep learning, image recognition, etc.

 

2.    Preparation and support of Clinical Trials
⦁    Input to Clinical Investigation Protocol (including review of clinical trial design, sample size calculation), eCRF, Clinical Study Report, etc.
⦁    Decide what data are needed to answer specific questions or problems
⦁    Support quality assurance of data collection including risk-based monitoring
⦁    Provide training non-statistician with statistical knowledge

 

3.    Regulatory issues
⦁    Update statistical analysis processes to any change in regulation
⦁    Support SOP preparation and update
 

Profile Description

 

⦁    Minimum 2-3 years’ experience in Biostatistics or SAS Programming
⦁    Bio-medical, bio-statistical or mathematical degree
⦁    Experience in statistical analysis for clinical trials
⦁    Experience with CDISC ADaM standard implementation 
⦁    Advance SAS programming knowledge (Base, Stat and Macro programming)
⦁    Additional analytical and programming skills on R, Phyton or PowerBI is a plus 
⦁    Good understanding of Good Clinical Practice and ICH Guidelines
⦁    Good oral and written communication skills
⦁    Team player, able to work in an international environment
⦁    Fluent in English  and preferably one other language
⦁    Ability to motivate in a dynamic environment
⦁    High personal integrity, with focus on quality and accuracy
⦁    Ability to function in a self-directed manner with a high degree of independence
 

Offer

 

We offer an interesting role in an end-to-end clinical and medical team, where you can learn from and collaborate with colleagues with various scientific backgrounds.
In this broad role, you will have a chance to impact in several ways, looking at improvements, innovation and creative thinking.

 

You will be coached and managed by our experienced Biostatistics Manager, and will have access to a broad spectrum or trainings to improve soft and hard skills, aligned with our core values of Care, Respect, Quality, Creativity and Integrity. Of course you can count on a competitive salary package. 

Contact Person

 

Please send your resume in English to Jan Swinnen, Talent Acq Lead EMEA

Terumo Europe is een belangrijke speler in de EMEA healthcare markt. We maken deel uit van Terumo Corporation (Japan) en produceren, verdelen & verkopen medisch materiaal. Het EMEA hoofdkwartier en productiefaciliteiten van Terumo Europe zijn gevestigd in Leuven (België). Onze saleskantoren zijn verspreid over de EMEA regio.

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