Senior Statistical Programmer - FSP

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Job Details

Job Overview:

• Senior Statistical Programmers required to work for Covance as a Lead Statistical Programmer on studies in Phases I-II
• You will be employed by Covance and work within our FSPx department 100% dedicated to one Sponsor
• Office based in in any of our European or South African offices or home based anywhere in Europe or South Africa
• You must have previous Lead experience as a Statistical Programmer within a biotech, CRO or pharma company
• Strong Oncology experience in Phases I and II would be an advantage
• Opportunities to develop and progress

Discover new opportunities to grow your career as a Covance FSP Senior Statistical Programmer. Covance FSP are looking to hire experienced Lead Statistical Programmers.

Our partner has an incredibly exciting and strong pipeline with over 45 ongoing oncology studies in Phases I and II. The position offers a strong support network, flexible working solutions and the opportunity to progress your career. If you are looking to strengthen your Lead expertise whilst gaining exposure to a pharmaceutical working environment this is a fantastic opportunity.

This is an incredibly exciting time to be joining Covance as we continue to grow and expand. This is a full-time home or office-based role anywhere within Europe or South Africa.

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:

Job Primary Functions

• Act as a Lead Programmer for projects
• Develop SAS programs for SDTM, ADaM, client-defined analysis datasets, Patient Profiles, Tables, Listings and Graphs in support of the Statistical Analysis Plan, posters, manuscripts, Integrated Summary of Safety (ISS) and Integrated Summary of Efficacy (ISE)
• Provide technical planning to include overseeing the set-up of key macros and SAS programs
• Represent Statistical Programming at internal and client meetings
• Act as a Statistical Programming consultant to clients and internal customers in related disciplines e.g. Clinical Data Management, Project Management and Medical Writing.
• Demonstrate excellent problem solving skills, a proactive approach and a willingness to make decisions on a regular basis.
• Ensure quality of personal work and the work of the team when acting as a Lead Programmer
• Prioritize personal workload and that of teammates; perform work with minimal supervision
• Work on complex problems where analysis of situations or data requires an evaluation of intangible variables; development of technical solutions to abstract problems which require the use of ingenuity and creativity
• Advise management team of changes in scope of projects to enable the timely development of change orders
• Good experience with CDISC standards including Define.xml files
• Review draft and final production runs for project to ensure quality and consistency
• Represent Statistical Programming during client audits ensuring study documentation is maintained and filed according to Covance processes
• Provide ongoing training and mentoring within Statistical Programming to ensure thorough knowledge of the processes used and the ongoing technical development.

Education/Qualifications:

• BSc, preferably in computing, life science, mathematical or statistical subject

Experience:

• Previous Lead experience as a Statistical Programmer within a biotech, CRO or pharma company
• Knowledge in all aspects of clinical trials from initial study set-up to study completion
• Full knowledge and understanding of the processes and procedures used within a Statistical Programming environment
• Able to identify training and development needs, opportunities for optimizing staff utilization and employing the most efficient practices
• Excellent organizational skills and the ability to delegate and prioritize work to meet tight deadlines while maintaining high standards
• Self motivation and ability to work independently with minimum direction
• Good interpersonal skills and the ability to communicate appropriately with all levels of staff and confidently with other disciplines and external clients
• A proactive approach to developing and maintaining effective working relationships with staff in other disciplines, often in other locations and in working to achieve consistent processes and standards across them
• A co-operative and team orientated approach
• Team leadership experience, as demonstrated by ability to organize and motivate project teams
• Candidates must be fluent in English 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.

Keywords:

Senior Statistical Programmer, Covance, Statistical programming, Chiltern, Covance, Phases I-IV, Programmer Analyst, Stats Programmer, Senior, Statistical Programmer, Lead, SAS Programmer, CDISC, ADaM, SDTM, Biostatistics, Senior Statistician, Statistician, Biostatistician, Statistics, Study Biostatistician, pharma, pharmaceutical, SAS, STAT, home based, pharma, pharmaceutical, home-based, flexible working, flexible location, home based, field based, home based EU Anywhere, anywhere in Europe, field-based, clinical analytics, FSP, FSPx, Functional Service Provision, United Kingdom, UK, Great Britain, England, Birmingham, Cambridge, Sheffield, Manchester, Alderley Edge, Scotland, Edinburgh, Wales, Swansea, Northern Ireland, Maidenhead, Reading, Berkshire, Austria, Belgium, Bulgaria, Czech Republic, France, Paris, Germany, Greece, Hungary, Ireland, Italy, Lithuania, Netherlands, Leiden, Poland, Portugal, Romania, Russia, Slovakia, South Africa, Bloemfontein, Spain, Ukraine, oncology, cancer, early clinical development, early phase, phase one, Phase I, Phase 1, PI, Phase Two, Phase II, Phase 2, PII.

Company

At Labcorp, we believe in the power of science to change lives. We are a leading global life sciences company that delivers answers for crucial health questions —because we know that knowledge has the potential to make life better for all. Through our unparalleled diagnostics and drug development capabilities, we provide insights and accelerate innovations that not only empower patients and providers but help medical, biotech, and pharmaceutical companies transform ideas into innovations. Here, you can join our more than 70,000 employees, serving clients in more than 100 countries, as we work together to make a real impact on people’s lives. Join us in our pursuit of answers.

Company info

Website
Location
Maidenhead Office Park
Westacott Way
Littlewick Green
Maidenhead
SL6 3QH
United Kingdom
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