Implement the statistical function’s role in the oncology compounds’ medical impact plans
Plan and execute evidence generation efforts, such as post-hoc analysis with innovative analytical approaches
Respond to payer and reimbursement needs
Review investigator initiated studies and design Phase IV studies as the study biostatistician
Ensure statistical rigor in all duties
Work with fellow clinical development biostatisticians and programmers to deep dive into clinical trial data
Collaborate with medical directors, HEOR, medical writing, market access, and other colleagues

PhD / DrPH in statistics/biostatistics or related disciplines with >2 years experience in the pharmaceutical/biotech industry or MS degree in statistics/biostatistics with >7 years’ experience in the pharmaceutical industry as a statistician
Knowledge of drug discovery/development/life cycle management(LCM)
Excellent influence and leadership skills
Demonstrated critical thinking skills, time management skills, and effective communication skills
Solid knowledge of statistical analysis methodologies, experimental and clinical trial design
Ability to write code in at least one common statistical software (i.e. SAS, R, Python)
Ability to read SAS code

health and wellness programs (including medical, dental, vision, life, and disability insurance)
fitness centers
401(k) company match
family support benefits
equity awards
annual bonuses
paid time off
paid leaves (e.g., military and parental leave)

Manager, Biostatistics – Medical Affairs

Key skills