Who is Aixial Group ?

Aixial Group, CRO (Clinical Research Organization), specialized in Life Science. We work with laboratories to provide technical support on clinical projects from phases I to IV and post market.

Since 2014, we have been part of the Alten family. We are developing our activities in Switzerland, France, Belgium, Czech Republic, Denmark, UK, US…with even more prospects for expanding internationally.

Aixial Group, operates in outsouring, insourcing, for pharmaceutical, cosmetic, medical device, biotechnology, nutrition,… activities in clinical operations, regulatory affairs, quality, biometrics, pharmacovigilance, HEOR…

Aixial Group continues to grow, and to recruit in the clinical trial professions. Come and join us, and discover our site to follow the news of our offers.

The Team of Aixial Group Switzerland is looking for his next Senior Biostatistician (M/F) !

You will design statistical methods and perform statistical analyses of study and clinical data. You will also be responsible for providing statistical input and managing all statistical activities for assigned projects/programmes, and for planning and managing statistical analyses according to project timelines.

ACTIVITIES :

• Provide statistics input into trial development activities such as study design, sample sizing and protocol
• Define and develop biostatistical methodologies for clinical, preclinical and epidemiological studies
• Draft statistical part of the protocol, study reports and articles
• Draft the statistical analysis plan
• Interpret and/or analyse the statistical results of preclinical and epidemiological clinical studies
• Determine the number of subjects required for clinical, preclinical and epidemiological studies, if necessary
• Propose statistical studies for clinical study development plans
• Validate clinical study protocols
• Manage subcontracting activities
• Monitor methods and/or tools
• Manage outsourced biometrics activities such as creation of SAP, ongoing data reviews, trial progress and reporting of clinical studies

REQUIREMENTS

• MSc or higher level in a statistics discipline
• > 7 years clinical trials experience
• Strong experience as statistician on clinical trials working with SAS, R
• Experience in the set-up and maintenance of data and programming standards, knowledge of CDISC standards
• Excellent communications skills in English
• Proactive and enthusiastic Team player
• Exposure to Medical Affairs activities
• Able to work independently

You are available in short time.

You are able to work in remote or be based in Switzerland.

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