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From the employer's careers site First seen 28 Oct 2026

Principal Biostatistician

Syneos Health senior full-time

The employer hasn't listed a salary.

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Description

Syneos Health is seeking a Principal Biostatistician to lead projects across multiple studies or programs. The successful candidate will act as the primary contact with the sponsor for all biostatistics-related activities on assigned projects.

Responsibilities:

  • Serve as a statistical department resource and mentor biostatisticians on job skills
  • Oversee or develop training plans or materials for Biostatistics associates
  • Direct the activities of other biostatistics personnel on assigned projects
  • Provide independent review of project work produced by other biostatisticians in the department
  • Prepare or oversee the preparation of Statistical Analysis Plans (SAPs)
  • Collaborate with sponsor, if required
  • Create or review programming specifications for analysis datasets, tables, listings, and figures
  • Review SAS annotated case report forms (CRFs), database design, and other study documentation
  • Implement company objectives and create alternative solutions to address business and operational challenges
  • Interface with other departmental project team representatives
  • Conduct and participate in verification and quality control of project deliverables
  • Manage scheduling and time constraints across multiple projects
  • Monitor progress on study activities against agreed-upon milestones
  • Provide statistical programming support as needed
  • Participate in Data Safety Monitoring Board (DSMB) and/or Data Monitoring Committee (DMC) activities
  • Maintain well-organized, complete, and up-to-date project documentation
  • Display willingness to work with others and assist with projects and initiatives as necessary

Requirements:

  • Graduate degree in biostatistics or related discipline
  • Extensive experience in clinical trials or an equivalent combination of education and experience
  • Proficiency in programming
  • Ability to apply extensive knowledge of statistical design, analysis, relevant regulatory guidelines, and programming techniques
  • Experience across all statistical tasks required to support clinical trials during the lifecycle of the project
  • Excellent written and verbal communication skills
  • Ability to read, write, speak, and understand English

Skills

Required

Nice to have

  • regulatory submissions
  • Data Safety Monitoring Board (DSMB)
  • Data Monitoring Committee (DMC)
Apply on Syneos Health