Biostatistics Lead, Oncology Trials

Jazz Pharmaceuticals, Inc.

Philadelphia (Philadelphia County)

Vor Ort

USD 172.000 - 258.000

Vollzeit

vor 10 Stunden
Sei unter den ersten Bewerbenden

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Benefits dieser Stelle

Medical, dental and vision insurance
401k plan with company match
Paid time off and holidays

Zusammenfassung

Jazz Pharmaceuticals seeks an Associate Director, Biostatistics to lead statistical activities across Phase I–IV programs. You will design analyses, shape statistical strategy, and collaborate with clinicians, data managers, statisticians, and programmers to ensure rigorous analyses and robust regulatory submissions.

You will also manage statisticians, supervise external vendors, and engage with regulatory agencies to advance development in oncology and neuroscience.

Qualifikationen

  • PhD or MS with extensive experience in statistics and clinical trial design.
  • Strong experience in oncology or hematology therapeutic areas.
  • Proficiency in SAS or R and regulatory submissions.
  • Solid knowledge of CDISC SDTM and ADaM standards.
  • Excellent communication and leadership abilities.
  • Ability to work in fast-paced cross-functional teams.

Aufgaben

  • Lead statistical input and strategy for clinical trials within a project(s).
  • Develop and review statistical analysis plans and data interpretations.
  • Coordinate with clinicians, data managers, and programmers to execute analyses.
  • Oversee external vendors and supervise internal statisticians.
  • Interact with regulatory agencies and contribute to submissions.

Kenntnisse

Clinical trial design
Statistical modeling
SAS or R
Oncology experience
Regulatory knowledge
Leadership
Communication

Ausbildung

PhD in statistics
MS in statistics

Tools

SAS
R
CDISC SDTM/ADaM

Jobbeschreibung

Jazz Pharmaceuticals seeks an Associate Director, Biostatistics to lead statistical activities across Phase I–IV programs. You will design analyses, shape statistical strategy, and collaborate with clinicians, data managers, statisticians, and programmers to ensure rigorous analyses and robust regulatory submissions.

You will also manage statisticians, supervise external vendors, and engage with regulatory agencies to advance development in oncology and neuroscience.

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