Senior Biomarker Biostatistician Genomics & Oncology

Syneos Health, Inc.

New York (NY)

Vor Ort

USD 180.000 - 230.000

Vollzeit

14 Tage+

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Maßgeschneiderter Lebenslauf und Anschreiben – versandbereit.

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Zusammenfassung

Syneos Health seeks a Principal Biostatistician (Biomarker Analyst) to lead biomarker statistics across global studies, including genomics and oncology. You will design SAPs, supervise teams, and ensure robust analyses for EMEA and US projects.

The role demands extensive clinical trials experience, strong programming skills, and clear communication with sponsors. Minimal travel may be required as projects demand.

Qualifikationen

  • Strong knowledge on Biomarker evaluation, esp. in Oncology and ctDNA data.
  • Excellent written and verbal communication; ability to lead multiple projects.
  • Proficiency in programming and statistical methods for clinical research.

Aufgaben

  • Collaborates with cross-functional teams to plan, execute and analyze biomarker aspects of studies.
  • Develops Biomarker Evaluation Plan ensuring consistency across projects.
  • Oversees statistical activities for biomarker R&D and projects; mentors staff.
  • Prepares SAPs and mock-up displays for tables, listings and figures; interacts with sponsor as needed.
  • Lead Biostatistician for protocol statistical aspects, randomization schedules, and CSR input.
  • Reviews programming specs, CRFs, and database design to ensure data quality for analyses.
  • Provides training and quality control to ensure timely, high-quality deliverables.
  • Participates in complex projects and regulatory interactions as needed.

Kenntnisse

Biomarker evaluation
Genomics analysis
Statistical programming
Leadership/mentoring
English communication

Ausbildung

Graduate degree in biostatistics
Experience in clinical trials

Tools

SAS and R programming

Jobbeschreibung

Syneos Health seeks a Principal Biostatistician (Biomarker Analyst) to lead biomarker statistics across global studies, including genomics and oncology. You will design SAPs, supervise teams, and ensure robust analyses for EMEA and US projects.

The role demands extensive clinical trials experience, strong programming skills, and clear communication with sponsors. Minimal travel may be required as projects demand.

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