Job Description

Key Responsibilities:

• Statistical Analysis:

  • Plan, supervise, implement, and monitor statistical processes for multiple clinical trials.
  • Apply advanced biostatistical methods and techniques to clinical trial data.

• Clinical Trial Design:

  • Collaborate on clinical trial design and scenario planning, ensuring statistical methodologies are aligned with regulatory requirements.

• Bayesian Statistics:

  • Utilize expertise in Bayesian statistics to enhance trial design and analysis.

• Statistical Software Proficiency:

  • Employ statistical software (SAS and/or R) for data analysis and reporting.

• Collaboration:

  • Work closely with program partners and stakeholders to deliver statistical outputs for one or more clinical trials.
  • Clearly communicate complex statistical concepts and findings in both written and verbal forms.

• Team Dynamics:

  • Act as a team player with a focused attitude, contributing to a collaborative work environment.
  • Work autonomously while integrating into a cross-disciplinary team in a fast-paced biotech setting.

Qualifications:

• Educational Background:

  • Master's degree or Ph.D. in Statistics or a related field.

• Experience:

  • Minimum of 6 years of experience in biostatistics, which may include doctoral research.
  • Demonstrated expertise in drug development and clinical trials within a regulatory environment.
  • Extensive experience in the Pharma or Biotech industry.

• Technical Skills:

  • Strong command of biostatistics and its application to clinical trials.
  • Proficiency in statistical software, particularly SAS and/or R.

• Soft Skills:

  • Excellent communication skills, with the ability to explain complex statistical concepts clearly.
  • Strong problem-solving abilities and a proactive approach to challenges.
  • Ability to work effectively both independently and as part of a team.

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