SEC Recruitment

Principal Biostatistician

Location
Switzerland
Posted
22 Feb 2021
Closes
22 Mar 2021
Ref
BIO/SW/PHARMA/2021
Contact
Yanick Millet
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)
Fantastic opportunity to join a Pharma company based in Switzerland as Principal Biostatistician.

Mission:

* Providing statistical support and input to the design and analysis of clinical studies.

* Responsible for the quality and timelines of all statistical and programming deliverable for assigned

* clinical studies, including studies for which statistical activities are outsourced to CRO partners.

* Ensuring timely availability of complete, accurate and consistent analysis results to support decision making

* Working as a key member of the clinical study team.


Your main responsibilities:

* Provide statistical input to the design, analysis and interpretation of clinical studies

* Author statistical sections of protocols and statistical analysis plans

* Ensure provision of quality and timely statistical analyses results that support quality and timely decision making

* Lead statistical and programming study teams and perform statistical analyses

* Coordinate and provide statistical oversight for outsourced studies, ensuring CROs accountability for the quality of their deliverable

* Represent statistics within cross functional study teams and provide statistical support and solutions

* Assist with in interactions with health Authorities

* Maintain current scientific and regulatory knowledge

* Provide input/lead internal process improvement

* Ensure adherence to GCP, regulatory guidelines, standard processes and SOPs.


Your profile:

* MSc. or PhD in statistics or related field

* Minimum of 4 years' experience as project/study statistician in Clinical Development in the pharmaceutical industry or CRO

* Strong statistical methodology knowledge and applications.

* Experience using Bayesian designs is a plus

* Excellent programming skill in SAS. Experience using R is a plus

* Good experience using CDISC standards

* Up to date knowledge of regulatory requirements related to statistics

* Good communication skills and ability to build positive relationships

* Fluent in English


To apply reach out:

Yanick Millet

TEL: +33 1 70 80 74 89
EMAIL: yanick.millet@secpharma.com

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