A global Clinical Research Organisation has an opening for a Senior Statistician to be based in its office in Chapel Hill, North Carolina. This is a fantastic opportunity to work for a growing organisation that empowers its employees to work autonomously and creatively, to retain and develop the company’s Centre of Excellence for Clinical Data Services.
The Company
Our client is an international CRO that specialises in clinical data including Biostatistics, Programming and Analysis, Clinical Data Management, Medical Writing, Pharmacovigilance and Clinical Technologies (EDC, ePRO, IWRS, CTMS). Working for global Pharmaceutical and Medical Device clients, the company supports large and small Phase I-IV drug development trials, offering a centralised clinical data approach alongside technology solutions that allow clients to view the status of studies in real-time.
The Position
As a Senior Statistician, you will have the opportunity to play an instrumental part in the Statistical Services provided to Sponsors within the US and internationally. Working as a part of a small team within the North Carolina office, but with the support of a larger global Statistics department, you will have the scope and responsibility to work independently on a wide range of statistical activities, including working as project lead on assigned studies.
Key responsibilities will include:
• Preparing and reviewing Statistical Analysis Plans and Specifications
• Writing statistical methodology and results sections of reports
• Providing statistical input to the design and review of Protocols and Case Report Forms
• Preparing and delivering training to staff and clients on statistical methodology and principles
• Supporting presentations to clients and managing the technical communications
• Reviewing statistical analyses (tables, figures and listings) and specifications of clinical trials
• Performing sample size calculations
Skills and Experience Required
• Preferably Masters Degree in Statistics but minimum Bachelor Degree in Statistics
• Substantial Statistical experience in a CRO, Pharmaceutical or Biotechnology environment
• Previous experience of working as Lead Statistician on studies
• Proven technical Statistics expertise
• Basic SAS programming skills
For further information please email [log in to unmask] with a copy of your current CV and a summary outlining your relevant experience.
Only candidates holding a valid EU work permit may apply as sponsorship is not offered. We try our best to respond to every application and you can be sure every single one will be reviewed, however due to the potential high volume of responses should you not hear back within 10 days from your application assume you have not been successful on this occasion.
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