Dear AllStat
My client, an expanding global CRO, is looking for a senior‐level professional able to work independently on requested activities, taking responsibility for the statistical outputs produced and overall Sponsor satisfaction, as well as oversee the work of junior resources they cooperate with.
The ideal candidate will work autonomously in preparing Statistical Analysis Plans and writing statistical methodology plans as well as the results sections of reports. He/she will also prepare and deliver training to staff and/or clients on statistical methodology and statistical principles.
Location: South East, United Kingdom (home‐based position negotiable)
Job Type: Permanent, Full‐time
Principal responsibilities include:
• Preparing and reviewing Statistical Analysis Plans
• Writing and reviewing statistical methodology and results sections of study reports
• Reviewing Statistical analyses (tables, figures and listings)
• Providing statistical input to the study design
• Reviewing Case Report Forms
• Writing Data Review plans and reports
• Writing and reviewing statistical parts of scientific articles
• Writing and reviewing DMC/DSMB charters and Reports
• Developing and validating SAS programs statistical analysis of study data finalized for the preparation of TLFs
• Programming and validating analysis datasets
• Developing SAS programs for the management of clinical study data (Datasets, mapping, pooling, import/export)
Ideal Candidate Profile:
• Bachelor’s degree in Statistics
• Relevant experience in biostatistics and statistical programming
• Good knowledge of SAS
• Very good knowledge of ICH E9 Statistical Principles for Clinical Trials
• Fluency in English
Interested candidates, please send your current CV to [log in to unmask]
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