Overview
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As Statistical Scientist Director, you will lead statistical strategy for key client studies, acting as primary liaison among sponsors and internal teams. You will shape design, analyses, and interpretation, and oversee statistical deliverables from protocol planning to reporting. You’ll translate complex quantitative concepts for non-statistical stakeholders and contribute to regulatory documents and publications. This role blends leadership, innovative design, and cross-functional collaboration to advance medical innovation. You will guide teams, mentor colleagues, and drive high-impact outcomes for patients and sponsors.
Compensaciones / Beneficios
flexible work arrangements
growth opportunities and mentorship
balance with life requirements
opportunity to contribute to life-saving therapies
travel opportunities (~20%)
collaborative, impact-driven culture
Responsabilidades
Lead statistician on complex client studies and drive project-level statistical strategy from protocol/SAP planning through reporting
Communicate quantitative concepts clearly to non-statistical stakeholders including sponsor leadership and regulatory representatives
Provide statistical input to Clinical Trial Reports and Protocols
Develop sample size, modeling approaches, adaptive or Bayesian trial designs
Oversee preparation of SAPs, randomization specifications, and statistical contributions to CSRs and regulatory documents




Collaborate with statistical programmers to ensure correct method implementation and interpretation
Independently develop SAS/R programs as needed
Identify design/analysis risks and propose mitigation strategies
Act as project manager for biostatistics work, managing budget, scope, and timelines
Ensure cross-project statistical consistency and contribute to portfolio-level strategy
Advise on regulatory guidelines and general expectations for submissions
Support business development through bid defenses and capabilities presentations
Provide internal consultancy on statistical issues and champion innovative methodologies
Mentor team members and support departmental training and SOPs
Act as biostatistician on DSMBs/DMCs
Perform other duties as assigned
Requisitos principales
15+ years’ experience in clinical trials design and analysis, preferably xqbhyrx in a CRO environment
1+ year of technical experience in innovative statistical designs in trials
Strong knowledge of regulatory, scientific, technical and clinical aspects in clinical trials within relevant therapeutic areas
Strong programming skills in SAS and R
Excellent working knowledge of CDISC standards and application
Ability to communicate statistical concepts to scientists and non-scientists
Experience interacting with regulatory agencies (FDA, EMA, etc.)
Proven ability to manage difficult stakeholder situations and ethical, data-driven decision making
Excellent English and host country communication skills
Willingness to travel (~20%)
clear communication
leadership and mentoring
stakeholder management
SAS
R
CDISC standards

📌 Statistical Scientist Director (Córdoba)
🏢 Premier Research
📍 Córdoba