Senior Biostatistician – Oncology (FSP -Permanent Homebased)

IQVIA Argentina; England; Remote; GBP 65,000 - 85,000; Full time

Job summary

A global clinical research firm is seeking an experienced Senior Biostatistician for a permanent remote position. You will lead on late-phase oncology trials and handle registrational studies and regulatory submissions. The ideal candidate has a Master’s or PhD in Biostatistics, at least 5 years of clinical trial experience, and strong SAS programming skills. Join us to make a high-impact on cancer treatment outcomes.

Benefits

Flexibility of remote work

Collaborative team environment

Exposure to cutting-edge oncology research

Qualifications

• 5+ years of experience in clinical trials with a focus on oncology.
• Proven experience working on registrational studies and regulatory submissions.
• Excellent communication skills and ability to work independently.

Responsibilities

• Serve as the lead statistician on global late-phase registration trials.
• Independently contribute to study design and statistical analysis plans.
• Address health authority questions and support responses with statistical analyses.

Skills

Biostatistics

SAS programming

Statistical analysis

CDISC standards

Communication skills

Education

Master’s or PhD in Biostatistics, Statistics, or related field

Tools

ADaM

SDTM

Job description

We are seeking an experienced and proactiveSenior Biostatisticianto join our FSP team, supporting a global pharmaceutical client. This is apermanent, home-basedposition offering the opportunity to work onlate-phase global oncology trials, with a focus onhematologyandregulatory submissions.

Key Responsibilities

• Serve as thelead statisticianon globallate-phase registration trials, particularly in oncology (hematology preferred).
• Independently contribute tostudy design,statistical analysis plans (SAPs), andregulatory submission strategies.
• Participate instudy team meetings, providing statistical guidance and collaborating with cross-functional teams.
• Addresshealth authority questionsand support responses with appropriate statistical analyses and documentation.
• Performhands-on statistical programmingto derive outputs and summary statistics usingADaMandSDTMdatasets.
• Ensure timely and accurate delivery of statistical deliverables in compliance with regulatory standards

Required Qualifications

• Advanced degree (Master’s or PhD) inBiostatistics,Statistics, or a related field.
• 5+ yearsof experience in clinical trials, with a strong focus ononcology(hematology and late-phase preferred).
• Proven experience working onregistrational studiesandregulatory submissions.
• Strong knowledge ofCDISC standards, particularlyADaMandSDTM.
• Proficiency inSASprogramming and ability to perform hands-on statistical analyses.
• Excellent communication skills and ability to work independently in a global, cross-functional environment.

Preferred Experience

• Prior involvement inFDA/EMA submissions.
• Experience addressingregulatory agency queries.
• Familiarity withreal-world evidenceandobservational studiesis a plus.

Why Join Us?

• Work onhigh-impact global studieswith a focus on improving cancer treatment outcomes.
• Be part of acollaborative and innovativeteam environment.
• Enjoy theflexibility of remote workwith a permanent contract.
• Gain exposure toregulatory strategyandcutting-edge oncology research.

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