• Hybrid role performing Statistical Programmer, Biostatistician and Clinical Data Manager tasks required to work for Covance
• You will be permanently employed by Covance and work within our FSPx department 100% dedicated to one Sponsor
• Office based or home based in Spain
• After a year you will have the opportunity to specialise into one of these three roles: Statistical Programming, Biostatistics or Clinical Data Management
• You must have previous experience working as a Statistical Programmer, Biostatistician and Clinical Data Manager within a biotech, CRO, device or pharma company
• Opportunities to develop and progress

What is FSP?

At Covance, you can redefine what is possible and discover your extraordinary potential within our Functional Service Provider team (FSP).

As a Covance employee dedicated to an FSP project you will bring your specialized discipline to a core team working directly with one sponsor. Whether your specialization is in clinical monitoring, clinical project management, data management, biometrics or pharmacovigilance Covance has an FSP opportunity to match your area of expertise.

Each FSP offers a unique opportunity to be a part of the drug development cycle and see a product through to launch. We have multiple partnerships giving you the variety and the flexibility to stay with sponsors, try a new external secondment or work in house on Covance studies.

With the support of exceptional people and an energized purpose, you'll be empowered to own your career journey with dedicated mentoring, training and personalized development planning. Further information can be found at: https://www.covance.com/services/functional-service-provision.html

Job Primary Functions

• Prepare and define statistical methods
• Participate in protocol design and CRF
• Write the data management plan
• Analyze data and present the data and clinical trial reports
• Perform statistical analysis and automatic verifications
• Write statistical reports for statistical sections and to provide statistical support across different teams

Education/Qualifications:

• Ideally BSc in a computing, life science, mathematical or statistical subject

Experience:

• Previous experience working as a Statistical Programmer, Biostatistician and Clinical Data Manager within a biotech, CRO, device or pharma company
• Positive attitude and willingness to learn and contribute in a team setting and communicate effectively within the team environment
• Good organization skills and the ability to prioritize own work
• Self motivation and ability to work independently
• A cooperative and team-oriented approach
• Candidates must be fluent in English and Spanish language (both verbal and written)

PLEASE NOTE CANDIDATES WHO DO NOT FULFIL THE CRITERIA MAY NOT RECEIVE A RESPONSE

NO AGENCIES PLEASE

MORE INFORMATION AVAILABLE ON REQUEST

For a confidential discussion about this opportunity, please phone Peter Lewis on +44 (0) 1628 543 457 . To apply, please click on the APPLY button.

About Covance:

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

Keywords:

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