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Amsterdam
2 days ago
Principal Biostatistician, FSP - Medical Affairs (m/w/d) logo

Principal Biostatistician, FSP - Medical Affairs (m/w/d)

IQVIA

Amsterdam
2 days ago
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Principal Biostatistician, FSP - Medical Affairs (m/w/d)

IQVIA is seeking a Principal Biostatistician to provide end-to-end statistical leadership and integration support across Phase II and Phase III studies in a fast-paced, global environment. The role involves leading SAP authoring and review, supporting integration activities, and acting as a proactive statistical partner to cross-functional teams. Strong experience as a Principal Biostatistician in Pharma or CRO, proven SAP expertise, and strong R programming skills are required.

RemoteFull-timePrincipalBiostatisticsSAP Authoring

Principal Biostatistician, FSP - Medical Affairs (m/w/d)

IQVIA is seeking a Principal Biostatistician to provide end-to-end statistical leadership and integration support across Phase II and Phase III studies in a fast-paced, global environment. The role involves leading SAP authoring and review, supporting integration activities, and acting as a proactive statistical partner to cross-functional teams. Strong experience as a Principal Biostatistician in Pharma or CRO, proven SAP expertise, and strong R programming skills are required.

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RemoteFull-timePrincipalBiostatistics

Salary

Not specified

Work Location

Amsterdam, North Holland, Netherlands, NL

Work Model

Remote

Employment Type

Full-time

Experience Level

Principal

Core Qualifications

Technical (Must-have)
BiostatisticsSAP authoringSAP reviewR ProgrammingPhase II clinical trialsPhase III clinical trialsStatistical integrationRegulatory compliance
Soft Skills
CommunicationIndependenceProactiveSolution-oriented

Preferred Qualifications

Technical (Nice-to-have)
Medical Affairs TA experience

Key Responsibilities

  • •Provide Principal-level Biostatistics support for Phase II–III clinical trials
  • •Independently lead SAP authoring and review
  • •Support integration activities across studies and programs
  • •Act as a proactive statistical partner to Clinical, Programming, and Regulatory teams
  • •Ensure delivery of high-quality, compliant statistical outputs within timelines
  • •Communicate clearly and confidently with internal and external stakeholders
BiostatisticianClinical ResearchPharmaCROPhase IIPhase IIISAPR ProgrammingMedical AffairsRemote
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