Principal Statistician

JD:

Statistical leader in the cross-functional development team of one compound/indication

Statistical expertise to the development strategy, decision making and interpretation of the data generated through the clinical development program, embracing excellence and innovation among quantitative methods

Closely collaborate with program partners and stakeholders to deliver on-time the statistical deliverables for all clinical trials and/or HA submissions of one compound/indication

Report to a disease area team leader, within the Biostatistics and Statistical Modelling organisation

Carry out functional responsibilities in accordance with applicable company guidelines and regulatory requirements

Desired Skills, Qualifications and Experience:

Master or doctorate (Ph.D.) degree in Statistics or related field with a minimum of 6 years’ experience (which may include doctoral research in field of biostatistics)

Expertise in drug development in a regulatory environment, with a demonstrated track record of advanced knowledge of biostatistics and strong command of its application to clinical trials

Experience in clinical trial design and scenario-planning

Extensive experience in the Pharma or Biotech environment

Demonstrates ability to plan, supervise, implement and monitor the statistical processes for multiple clinical trials

Expertise in Bayesian statistics

Proficient in statistical software (SAS and/or R);

Able to collaborate with program partners and stakeholders to deliver on the statistical deliverables for one or more clinical trials

Clearly explain complex statistical concepts in written and spoken English and not afraid to contribute and speak up when necessary

Team-player with focused attitude

Able to work autonomously as part of a cross-disciplinary team in a dynamic surrounding of a fast growing biotech company with challenging timelines