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- Tasks: Lead statistical support for oncology studies, ensuring data quality and regulatory compliance.
- Company: Proclinical is a top life sciences recruiter connecting talent with global opportunities.
- Benefits: Enjoy a fully remote role with flexible working hours and a supportive team environment.
- Why this job: Join a dynamic team making a real impact in oncology research with innovative methodologies.
- Qualifications: Master's in Biostatistics or Statistics required; Ph.D. preferred, with strong SAS and R skills.
- Other info: This permanent position is open to candidates based in the UK or France.
The predicted salary is between 43200 - 72000 £ per year.
Are you a dedicated individual looking to put your expertise to work fully flexibly in a remote position? Proclinical is seeking a Lead/Principal Statistician to provide strategic support and leadership within a cross-functional team focused on oncology studies. This role involves contributing to study design, protocol development, and statistical analysis plans, ensuring high-quality data management and regulatory compliance. You will act as the statistical expert for clinical development programs, employing advanced methodologies and innovative trial designs. This permanent position is fully remote based within United Kingdom or France.
Responsibilities:
- Provide statistical expertise in study design and protocol development.
- Conduct sample size and power calculations, and simulations.
- Develop statistical analysis methodologies and plans.
- Oversee blinded in-trial data quality review and pre-database lock data control.
- Support the development of table, listing, and figure templates.
- Manage programming and production tasks.
- Oversee contract or CRO resources.
- Prepare and document clinical regulatory submission packages.
- Ensure adherence to CDISC standards and regulatory requirements.
- Collaborate effectively with multidisciplinary teams and external agencies.
Key Skills and Requirements:
- Expertise in oncology clinical development and regulatory submissions.
- Strong knowledge of statistical theory and methods.
- Proficiency in SAS and R programming for data management and analysis.
- Excellent communication, leadership, and intercultural skills.
- Ability to make informed decisions in ambiguous situations.
- Proficiency in MS Word, Excel, and PowerPoint.
- Sound understanding of clinical and statistical regulatory requirements (e.g., GCP, ICH, CDISC).
- Master's degree in Biostatistics or Statistics; Ph.D. preferred.
If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.
Contact Detail:
Job Traffic Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Lead Statistician/Principal Statistician - Oncology
✨Tip Number 1
Network with professionals in the oncology field. Attend relevant conferences or webinars to connect with industry experts and learn about the latest trends. This can help you gain insights into what employers like us at StudySmarter are looking for.
✨Tip Number 2
Familiarise yourself with the latest statistical methodologies and tools used in oncology studies. Being well-versed in advanced techniques will not only boost your confidence but also demonstrate your commitment to staying current in your field.
✨Tip Number 3
Prepare to discuss your previous experiences in leading cross-functional teams. Highlight specific projects where you contributed to study design and protocol development, as this will showcase your leadership skills and expertise in a practical context.
✨Tip Number 4
Brush up on your knowledge of regulatory requirements such as GCP, ICH, and CDISC standards. Being able to speak confidently about these topics during interviews will set you apart from other candidates and show that you understand the compliance landscape.
We think you need these skills to ace Lead Statistician/Principal Statistician - Oncology
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your expertise in oncology clinical development and statistical methodologies. Emphasise your experience with SAS and R programming, as well as any relevant leadership roles you've held.
Craft a Strong Cover Letter: In your cover letter, express your passion for oncology studies and how your skills align with the responsibilities outlined in the job description. Mention specific examples of your contributions to study design and protocol development.
Highlight Relevant Skills: Clearly list your proficiency in statistical theory, data management, and regulatory compliance. Make sure to include your understanding of CDISC standards and any experience with clinical regulatory submissions.
Proofread Your Application: Before submitting, carefully proofread your application materials for any errors or inconsistencies. A polished application reflects your attention to detail, which is crucial for a statistician role.
How to prepare for a job interview at Job Traffic
✨Showcase Your Statistical Expertise
Be prepared to discuss your knowledge of statistical theory and methods, especially in the context of oncology. Highlight any relevant experience you have with study design and protocol development, as this will demonstrate your capability to contribute effectively to the role.
✨Demonstrate Programming Proficiency
Since proficiency in SAS and R is crucial for this position, be ready to provide examples of how you've used these tools in past projects. Discuss specific statistical analyses you've conducted and how they contributed to successful outcomes.
✨Emphasise Leadership and Collaboration Skills
This role requires strong leadership and the ability to work within multidisciplinary teams. Prepare examples that showcase your leadership experience and how you've successfully collaborated with others, particularly in high-pressure or ambiguous situations.
✨Understand Regulatory Requirements
Familiarise yourself with clinical and statistical regulatory requirements such as GCP, ICH, and CDISC standards. Be ready to discuss how you ensure compliance in your work, as this will be a key aspect of the role.
