Principal Biostatistician (f666)

  • Contract Duration: 12+ Months, Hybrid
  • Research & Development
  • Cambridge, MA

Website Lenox Executive Search

Job description

12+ month CONTRACT role. Hybrid role – some onsite work in Cambridge required so candidates must be LOCAL to Boston area. Urgent need – ASAP START! Max pay rate 78.00/hour.

Lenox Executive Search is seeking an experienced Principal Biostatistician to fill an 12+ month extendable contractual role with a global pharmaceutical company in Cambridge, MA. Must have Master or doctorate (Ph.D.) degree in Statistics or related field with 6+ years experience (which may include doctoral research in field of biostatistics).

REQUIREMENTS for the Principal Biostatistician:

  • Master or doctorate (Ph.D.) degree in Statistics or related field
  • 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

RESPONSIBILITIES of the Principal Biostatistician:

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

Job Types: Full-time, Contract

Pay: $78.00 per hour

Expected hours: No less than 40 per week

Schedule:

  • 8 hour shift
  • Monday to Friday

Education:

  • Master’s (Required)

Experience:

  • Statistical: 6 years (Required)
  • Pharma/Biotech industry: 2 years (Required)
  • SAS and/or R statistical software: 3 years (Required)
  • Bayesian statistics: 2 years (Preferred)

Ability to Relocate:

  • Cambridge, MA 02139: Relocate before starting work (Required)
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