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Principal / Senior Principal Biostatisticians (Phases II-IV & Statistical Analysis Research Centre)

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Location(s): Anywhere in Europe, Permanent
Salary: Competitive salary and company benefits apply

Covance, the drug development business of LabCorp, is recognized as a leader in drug development because of our exceptional people.  At Covance, we embrace and celebrate the different strengths, experiences and perspectives of our 20,000+ team members across the globe.  Our team is driven by an energizing purpose to improve health and improve lives.  Here, you can play a role in bringing new scientific discoveries to life and make a difference in the lives of millions.  And, with our comprehensive service portfolio, you’ll have the opportunity to explore diverse projects and unique career paths across the drug development spectrum.  Join us and discover your extraordinary potential.  



ROLES AVAILABLE

*Principal / Senior Principal Biostatisticians (Phases I-IV)

Join our growing team and discover your extraordinary potential by working as a Covance Senior or Senior Principal Biostatistician.  You will enjoy a varied role working for different sponsors across several therapeutic areas, leading projects and mentoring junior members of the department.  The position offers an excellent support network with access to Covance’s statistical consultants, flexible working solutions and the opportunity to progress your career.  If you are looking to strengthen your expertise within a varied and dynamic environment, then this is a fantastic opportunity.  

You will have a Master’s degree, equivalent, or higher in Biostatistics or related field.  Previous experience of working as a Senior or Principal Biostatistician in either a biotech, CRO or pharma company essential.




*Senior Principal Biostatisticians (Statistical Analysis Research Centre)

Join our growing team and discover your extraordinary potential by working as a Covance Senior Principal Biostatistician within our SARC (Statistical Analysis Research Centre) team.  The SARC team is a service group within Covance that can provide statistical expertise, statistical consulting, or independent statistical review for clinical protocol design to regulatory submissions.   Within the SARC team, we have very talented set of individuals with many years of statistical and pharmaceutical expertise in all phases of clinical development and several therapeutic areas.

In this role you will consult in the design of complex and innovative studies and clinical trial programs as well as Leading the DMC/DSMB processes.  

You will have a Master’s degree, equivalent, or higher in Biostatistics or related field and be able to demonstrate good knowledge in supporting data monitoring committees with excellent organizational skills, communication skills and writing skills.  In addition, you will have a broad up-to-date knowledge of statistics as applied in clinical trials across therapeutic areas and to complex statistical methods (including adaptive design and platform trial design).


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For more information on Covance please visit: www.covance.com.