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- Tasks: Lead global oncology trials and contribute to study design and statistical analysis.
- Company: Join a leading global provider of clinical research services.
- Benefits: Permanent home-based role with flexible work options and competitive salary.
- Why this job: Make a real impact on cancer treatment outcomes through innovative research.
- Qualifications: Advanced degree in Biostatistics and 5+ years in clinical trials, especially oncology.
- Other info: Collaborative team environment with opportunities for professional growth.
The predicted salary is between 48000 - 72000 £ per year.
We are seeking an experienced and proactive Senior Biostatistician to join our FSP team, supporting a global pharmaceutical client. This is a permanent, home-based position offering the opportunity to work on late-phase global oncology trials, with a focus on hematology and regulatory submissions.
Key Responsibilities
- Serve as the lead statistician on global late-phase registration trials, particularly in oncology (hematology preferred).
- Independently contribute to study design, statistical analysis plans (SAPs), and regulatory submission strategies.
- Participate in study team meetings, providing statistical guidance and collaborating with cross-functional teams.
- Address health authority questions and support responses with appropriate statistical analyses and documentation.
- Perform hands-on statistical programming to derive outputs and summary statistics using ADaM and SDTM datasets.
- Ensure timely and accurate delivery of statistical deliverables in compliance with regulatory standards.
Required Qualifications
- Advanced degree (Master’s or PhD) in Biostatistics, Statistics, or a related field.
- 5+ years of experience in clinical trials, with a strong focus on oncology (hematology and late-phase preferred).
- Proven experience working on registrational studies and regulatory submissions.
- Strong knowledge of CDISC standards, particularly ADaM and SDTM.
- Proficiency in SAS programming 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 in FDA/EMA submissions.
- Experience addressing regulatory agency queries.
- Familiarity with real-world evidence and observational studies is a plus.
Why Join Us?
- Work on high-impact global studies with a focus on improving cancer treatment outcomes.
- Be part of a collaborative and innovative team environment.
- Enjoy the flexibility of remote work with a permanent contract.
- Gain exposure to regulatory strategy and cutting-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.
Senior Biostatistician – Oncology (FSP -Permanent Homebased) employer: IQVIA Argentina
Contact Detail:
IQVIA Argentina Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Biostatistician – Oncology (FSP -Permanent Homebased)
✨Tip Number 1
Network like a pro! Reach out to your connections in the biostatistics and oncology fields. Attend industry events or webinars, and don’t be shy about asking for informational interviews. You never know who might have the inside scoop on job openings!
✨Tip Number 2
Prepare for those interviews! Research the company and their recent projects, especially in oncology. Be ready to discuss your experience with regulatory submissions and statistical programming. Practise common interview questions so you can showcase your skills confidently.
✨Tip Number 3
Showcase your expertise! Create a portfolio of your work, including any relevant statistical analyses or projects you've contributed to. This will help you stand out and demonstrate your hands-on experience in late-phase global trials.
✨Tip Number 4
Apply through our website! We love seeing candidates who are genuinely interested in joining our team. Make sure to tailor your application to highlight your experience in oncology and regulatory submissions, and let us know why you're excited about this opportunity!
We think you need these skills to ace Senior Biostatistician – Oncology (FSP -Permanent Homebased)
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your experience in oncology and clinical trials. We want to see how your background aligns with the role, so don’t be shy about showcasing your relevant skills and achievements!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re passionate about biostatistics in oncology and how you can contribute to our team. Keep it engaging and personal – we love to see your personality come through.
Showcase Your Technical Skills: Since this role involves hands-on statistical programming, make sure to highlight your proficiency in SAS and your knowledge of CDISC standards. We’re looking for someone who can hit the ground running, so let us know what you can do!
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it’s super easy – just follow the prompts and you’ll be all set!
How to prepare for a job interview at IQVIA Argentina
✨Know Your Stats
Brush up on your biostatistics knowledge, especially in oncology and hematology. Be ready to discuss specific statistical methods you've used in past trials and how they contributed to successful outcomes.
✨Familiarise with Regulatory Standards
Make sure you understand CDISC standards and regulatory submission processes. Prepare examples of how you've navigated these in previous roles, as this will show your expertise and readiness for the position.
✨Showcase Your Communication Skills
Since you'll be collaborating with cross-functional teams, practice articulating complex statistical concepts in simple terms. This will demonstrate your ability to communicate effectively with non-statistical colleagues.
✨Prepare for Scenario Questions
Anticipate questions about how you'd handle specific challenges in late-phase trials or regulatory submissions. Think through your problem-solving strategies and be ready to share relevant experiences that highlight your proactive approach.
