Senior/Principal Biostatistician

IQVIA; Modena; Ibrido; EUR 45.000 - 70.000; Tempo pieno

Descrizione del lavoro

IQVIA seeks a Senior/Principal Biostatistician to join their innovative team, offering global project exposure and career development. Responsibilities include statistical consulting, leading studies, and collaborating on clinical trial outcomes. The role provides access to cutting-edge technology in a supportive environment, fostering work-life balance.

Servizi

Global exposure

Variety of therapeutic areas

Collaborative team environment

Access to cutting-edge technology

Excellent career development opportunities

Work-Life Balance

Competenze

• 5-7 years of relevant experience in clinical trials.
• Familiarity with moderately complex statistical methods.
• Experience with Phase 2/3 trials.

Mansioni

• Provide statistical consulting and technical support for clinical trials.
• Manage scope of work, budget, and forecasts.
• Collaborate with medical and programming staff on clinical trial reports.

Conoscenze

Statistical consulting

Communication of statistical concepts

Project management

Formazione

BSc or MSc in Biostatistics

Strumenti

SAS

Descrizione del lavoro

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IQVIA

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EU work permit required:

Yes

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Job Reference:

e02f7a6f366e

Job Views:

3

Posted:

10.07.2025

Expiry Date:

24.08.2025

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Job Description:

Home-Based/Hybrid/Office-Based

Join us on our exciting journey!

Improving the expectations for human health isn’t easy, but we are determined. Together, we are on a path to achieving this vision. At IQVIA, we share a passion for the greater good, a collaborative spirit, and endless curiosity. Each day is another opportunity to find new solutions and enable the next breakthrough.

Due to continued growth, we are seeking Senior/Principal Biostatisticians to join our award-winning and innovative department. You will have the opportunity to work globally and across a variety of therapeutic areas.

Job Overview:

As a Senior/Principal Biostatistician, you will have access to cutting-edge, in-house technology and opportunities to work on global projects across various therapeutic areas.

Thanks to our development opportunities and mentoring at all levels, you will be able to progress your long-term career in the direction you choose.

You will provide statistical consulting and technical support related to the design, analysis, and regulatory submissions of clinical trial studies.

Acting as a statistical team lead for complex studies or groups of studies, you will manage scope of work and budget, provide revenue and resource forecasts, and participate in proposal writing and bid defense meetings.

You will collaborate with medical and programming staff to produce interim and final reports, facilitating comprehensive understanding and interpretation of clinical trial data and outcomes.

Requirements:

BSc or MSc degree in Biostatistics or related field, with 5-7 years of relevant experience.

Familiarity with moderately complex statistical methods applicable to clinical trials.

Experience with Phase 2/3 trials.

Good working knowledge of SAS.

Ability to manage multiple tasks and projects effectively, and to communicate statistical concepts clearly.

What is in it for you?

Global exposure

Variety of therapeutic areas

Collaborative and supportive team environment

Access to cutting-edge in-house technology

Excellent career development and progression opportunities

Work-Life Balance

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 improve patient outcomes and population health worldwide. Learn more at our website.