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Statistical Analyst
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Proclinical is excited to announce that an exciting opportunity has arisen for a Statistical Analyst to join a scientifically driven, global, full-service clinical contract research organisation (CRO). The company provides Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries.
The Statistical Analyst will join the company on a full-time basis, and be stationed in their team in Belgium.
Job Responsibilities:
- Writing statistical programs for use in creating analysis datasets, tables, listings, and figures.
- Reviewing analysis plans for appropriate methods.
- Programming study analyses and reviewing study results.
- Communicating the project requirements for cleanup and data capture to ensure the key study variables are suitable for analysis.
Skills and Requirements:
- A Masters' degree.
- Demonstrable industry working experience with SAS programming or SAS certificates.
- Proven knowledge of databases and data management processes.
- Proven knowledge of statistical methods commonly used in pharmaceutical clinical trials.
- Excellent organisational and communication skills.
- Strong interpersonal skills, with an ability to interact cross-functionally and at all levels of the organisation.
- Excellent written, verbal communication, and presentation skills.
To Apply:
Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.
In case you have difficulty in applying or if you have any questions, please call Theodora Savlovschi-Wicks on +44 0203 752 0314 or upload your CV on our website - www.Proclinical.com.
A full job description is available on request.
Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
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