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Manager Biometrics (Belgium)

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 james@stelfoxuk.com

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