Rare opportunity to join one of the most prestigious and well respected
pharmaceutical companies across the globe.
Working on various Oncology compounds and trials you will be responsible for
the statistical support of Phase 1 through Phase 3 studies. This includes
contributing to the Clinical Development Plan, design and analysis of
trials, protocol development, randomization, e-CRF review, writing
Statistical Analysis Plans, report writing and statistical method
development, and take part in cross-functional working groups and in
meetings with the pharmaceutical regulatory authorities (e.g. FDA, EMEA).
Qualifications:
• Master or PhD in statistics or biostatistics with experience in early
and/or late phase clinical research and development.
• Candidate should have a proven track record within clinical statistics
with either a PhD or MSc.
• Good communication, presentation, organizational, project management and
problem-solving skills.
• Ability to work independently and effectively in a team environment and to
communicate with non-statisticians about statistical findings is necessary.
• Sound knowledge of SAS.
• Experience of protocol development and writing Statistical Analysis Plans,
reports and other documents in English.
If you would like more information on this role or would like to hear more
on the Biometric opportunities with Stelfox then please call 01273 727930
alternatively please send your CV to [log in to unmask]
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