7 publicaciones de empleo destacadas de representative (madrid) en el pardo madrid madrid provincia (¡Están contratando!)

Principal Biostatistician (Oncology) - FSP
IQVIA —Madrid, Madrid provincia
- Jornada completa
- Control de calidad
- Habilidades de comunicación
- Teletrabajo opcional
System Integration Manager (Fix-Term)
KION Group AG —Coslada, Madrid provincia
- Jornada completa
- Español
Senior Cyber Risk Consultant
Allianz —Madrid, Madrid provincia
- De 59.687 € a 72.951 € al año
- Jornada completa
- Trabajo híbrido
- Español
- Informática
- Inglés
- Plan de pensiones
Senior Data Research Analyst (Portuguese speaker)
Morningstar —Madrid, Madrid provincia
- De 38.000,00 € a 50.666,66 € al año
- Jornada completa
- Trabajo híbrido
- Español
- Microsoft Excel
- Inglés
PH Senior Engineer
Arup —Madrid, Madrid provincia
- Trabajo híbrido
- Inglés
- Oficina
- Liderazgo
Sales Development Representative (German/English Speaker)
Commvault —Madrid, Madrid provincia
- Ventas
- Inglés
- Microsoft Office
Sales Development Representative (SDR) Ventas · Madrid · Híbrido
FLOWww —Madrid, Madrid provincia
- Trabajo híbrido
- CRM software
- Ventas
- Inglés
- Formación continua
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Principal Biostatistician (Oncology) - FSP

IQVIA -
Madrid, Madrid provincia

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Jornada completa

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Teletrabajo opcional

Cualificaciones

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Descripción completa del empleo

Madrid, Spain | Full time | Home-based | R1560482

As a Principal Biostatistician, you will provide strategic statistical leadership for Oncology clinical trials, with a particular focus on hematological malignancies including multiple myeloma, leukemia, and lymphoma. You will work closely with cross-functional teams to deliver high-quality statistical support across the clinical development lifecycle, ensuring compliance with regulatory and industry standards.

Key Responsibilities

Provide Principal-level Biostatistics leadership for Oncology clinical development programs and studies
Lead and contribute to statistical activities across clinical trials, acting as the primary statistical representative on assigned studies
Review and provide quality control oversight of SDTM datasets and associated deliverables, ensuring compliance with CDISC standards
Collaborate closely with Statistical Programming, Data Management, Clinical Operations, and Regulatory teams to ensure accurate and timely delivery of statistical outputs
Support the interpretation and communication of study results to cross-functional stakeholders
Ensure all statistical deliverables meet quality, regulatory, and timeline expectations
Effectively communicate statistical concepts, analyses, and recommendations to both technical and non-technical audiences
Contribute to study design discussions, protocol development, and statistical methodology as required

Candidate Requirements

✔ Advanced experience as a Principal Biostatistician within a Pharmaceutical, Biotechnology, or CRO environment
✔ Strong experience within Oncology clinical development
✔ Demonstrated expertise in hematological malignancies, including multiple myeloma, leukemia, and/or lymphoma
✔ Strong knowledge and practical application of CDISC standards, including SDTM
✔ Experience performing or overseeing QC of SDTM datasets and related outputs
✔ Proven ability to work effectively within cross-functional teams and influence key stakeholders
✔ Excellent verbal and written communication skills
✔ Strong understanding of statistical principles and clinical trial methodology

Preferred Qualifications

✔ Experience serving as Lead Study Statistician within a cross-functional clinical development team
✔ Knowledge and experience in clinical trial statistical design and study planning
✔ Experience supporting regulatory submissions and interactions with health authorities
✔ Familiarity with advanced statistical programming tools and industry-standard processes

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Where you'll work

Home-based

You’ll work remotely, with the flexibility to do your best work from home. Supported by collaborative tools and a global team, you’ll stay connected while enjoying the autonomy and balance that comes with a fully remote role.

Culture

Culture at IQVIA is built on a shared belief: that when people are empowered with better data, smarter technology and deeper expertise, they can change what’s possible for patients. Across every team and every corner of the globe, you’ll find colleagues who genuinely care — about the mission and about each other. That’s what makes this a place where people tend to stay, grow and do the best work of their careers.

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