Senior COA/PRO Analytics Consultant - Remote

Profile Software Services

Lugo

Híbrido

EUR 90.000 - 130.000

Jornada completa

Hace 3 días
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Descripción de la vacante

IQVIA seeks a Senior Consultant to lead or support statistical analyses for COA/PRO data across drug development projects. You will contribute to planning, execution, interpretation, and reporting while communicating results to clients and internal teams.

The role emphasizes advanced methods, regulatory relevance, and collaboration across global teams. Remote work options are available, with a strong focus on scientific rigor and impact.

Formación

  • Master’s degree or PhD in biostatistics, statistics, psychometrics, outcomes research, epidemiology, or related quantitative field.
  • 5+ years of relevant experience in pharmaceutical, biotech, CRO, healthcare, or consulting.
  • Advanced knowledge of complex statistical methods for Phase I-IV clinical trials; SAS and/or R familiarity.

Responsabilidades

  • Lead the quantitative analysis workstream for projects of moderate complexity with high-quality delivery.
  • Develop and review analysis plans, output shells, programming requirements, and statistical reports.
  • Apply advanced statistical methods to COA/PRO data.
  • Interpret results clearly for internal teams and clients and justify methodological choices.
  • Contribute to regulatory- and payer-relevant evidence generation and scientific communication.
  • Build relationships with clients and cross-functional teams; participate in proposals and business development.
  • Assist in managing the scope, timelines, and quality of deliverables; mentor junior members.

Conocimientos

Statistical analysis leadership
COA/PRO data analysis
Regulatory understanding
Client communication
Mentoring teammates

Educación

Master’s degree or PhD in biostatistics / statistics / psychometrics / outcomes research / epidemiology

Herramientas

SAS
R

Descripción del empleo

IQVIA seeks a Senior Consultant to lead or support statistical analyses for COA/PRO data across drug development projects. You will contribute to planning, execution, interpretation, and reporting while communicating results to clients and internal teams.

The role emphasizes advanced methods, regulatory relevance, and collaboration across global teams. Remote work options are available, with a strong focus on scientific rigor and impact.

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