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Manager, Biostatistics (Real World Evidence: Home-Based/Hybrid)

Aplica ya
Mapa de ubicación: Oeiras, Lisbon, Portugal Full time R1154815

Descripción del trabajo

Manager, Biostatistics (Real-World Evidence)

Join us on our exciting journey!

Home-Based/Hybrid: Portugal, Greece, Estonia, Latvia, Spain & UK.

IQVIA™ Real-World Evidence (RWE) teams work with clients to help them collect and use real-world data to generate evidence to meet the needs of regulators, payers, providers, and patients.

Our approach is unique in the industry and is defining the way companies develop and apply real-world evidence for healthcare decision making.

We are collaborative, intellectually curious, entrepreneurial, and constantly looking for opportunities to harness the value of real-world evidence in an evolving industry.

We have one of the largest Biostatistics departments within the industry and due to continued growth, we are seeking new brave minds to join our innovative department.

Job Overview:

As a Manager for the Biostatistics department, you will be given access to cutting-edge in-house technology and provide direction and guidance in carrying out project assignments, interfacing with clients and other internal departments, and applying statistical methods to project work.

With site/staff level of visibility, you will manage a team of Biostatistics staff and provide training, guidance, and mentorship to staff members.

Along, with communicating on project progress, staffing concerns, including resource allocation with the Director, Biostatistics

You will perform expert reviews and participate as senior statistician on major projects, including developing/reviewing protocols, preparing analysis plans, overseeing the conduct of analyses, and preparing integrated clinical and statistical reports.

Requirements:

  • BSc or MSc degree in Biostatistics or related field and between 5-7 years’ relevant experience within the life-science industry, along with at least 1-year experience in supervising/managing staff

  • Familiarity with most complex statistical methods that apply to Phase I-IV clinical trials

  • In-depth knowledge of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines

  • Familiarity with moderately complex statistical methods that apply to applicable clinical trials

  • Strong working knowledge of SAS

JOIN US

Embrace your curiosity and grow your career in an exciting environment where development is a priority.

Think boldly and disrupt conventional thinking.

Enjoy what you do.

Whatever your career goals, we are here to ensure you get there!

At IQVIA, we believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. The advanced analytics, technology solutions and contract research services we provide to the life sciences industry are made possible by our 70,000+ employees around the world who apply their insight, curiosity and intellectual courage every step of the way. Learn more at jobs.iqvia.com.

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