Lead Biostatistician

i-Pharm ConsultingGruppe; España; Híbrido; EUR 30.000 - 50.000; Jornada completa

Descripción de la vacante

A leading global CRO is seeking a Lead Biostatistician to influence trial design and execution across EMEA studies. The candidate will manage statistical strategy, collaborate cross-functionally, and ensure quality and timelines. A Master’s degree in Statistics with 8-10 years industry experience is required. Strong SAS skills and team leadership are essential. This role offers remote options within the EU.

Formación

• 8–10 years’ industry experience (CRO/pharma, ideally with sponsor exposure).
• Proven experience leading cross-functional teams.
• Solid study design and regulatory exposure; immunology preferred.

Responsabilidades

• Lead statistical strategy and study design for clinical trials.
• Advise on protocols, SAPs, randomisation, and outputs.
• Collaborate with programming, data management, and cross-functional teams.

Conocimientos

Strong SAS programming skills

Proactive communication

Decision-making skills

Educación

Master’s degree in Statistics or Biostatistics

Descripción del empleo

Overview

Location: Remote (EU Wide, with flexibility to travel)

Contract: 6 months, (Inside IR35 for UK-based candidates)

Shape the Future of Clinical Trials

We’re partnering with a global CRO to hire Lead Biostatisticians to lead statistical strategy across complex EMEA studies. Work at indication-level or therapeutic area–wide (neurology, rheumatology, nephrology, endocrinology, haematology) and directly influence trial design, execution, and delivery.

The Role

• Lead statistical strategy and study design for clinical trials
• Advise on protocols, SAPs, randomisation, and outputs
• Oversee and validate tables, listings, and reports
• Collaborate with programming, data management, and cross-functional teams
• Act as the key statistical contact for sponsors
• Stay hands-on while guiding projects to meet quality, timelines, and budgets

About You

• Master’s degree in Statistics, Biostatistics, or related field
• 8–10 years’ industry experience (CRO/pharma, ideally with sponsor exposure)
• Strong SAS/programming skills; eCRT and Define knowledge a plus
• Proven experience leading cross-functional teams
• Solid study design and regulatory exposure; immunology preferred
• Proactive communicator with strong technical and decision-making skills

Why Join?

Make a tangible impact on meaningful studies across EMEA while advancing your leadership in biostatistics. Join a collaborative, hands-on environment where your expertise directly shapes clinical research.

Apply Now

Bring your expertise where it matters most. Lead, influence, and deliver results with a global CRO shaping the future of clinical trials.

Please note: You must be able to work in the UK without restriction or sponsorship to be eligible for this role. If you are interested in finding out more about this role or others, please contact Jada Kirlew at [e-mail] or call: [phone] / [phone] (NL)

• Location Melbourne, Victoria, Australia (Remote)
• Perth, Western Australia, Australia (On-site)