#699-Principal/ Senior Statistician Consultant- Late Phase Oncology (Remote in EU/UK)
#699-Principal/ Senior Statistician Consultant- Late Phase Oncology (Remote in EU/UK)

#699-Principal/ Senior Statistician Consultant- Late Phase Oncology (Remote in EU/UK)

Full-Time 42000 - 84000 £ / year (est.) No home office possible
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At a Glance

  • Tasks: Lead statistical analysis for late-phase oncology studies and mentor junior statisticians.
  • Company: Join ClinChoice, a global CRO dedicated to quality and professional growth in clinical development.
  • Benefits: Enjoy remote work flexibility, career advancement opportunities, and a supportive team culture.
  • Why this job: Make a real impact in drug development while working with diverse teams and innovative projects.
  • Qualifications: MS or PhD in Statistics/Biostatistics with relevant experience in clinical trials and FDA regulations.
  • Other info: ClinChoice values diversity and inclusivity, fostering a collaborative environment for all employees.

The predicted salary is between 42000 - 84000 £ per year.

#699-Principal/ Senior Statistician Consultant- Late Phase Oncology (Remote in EU/UK)

Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says it’s the best of both worlds….

ClinChoice is searching for a Senior/Principal Statistician Consultant- Onco Late Phase to join one of our clients.

ClinChoice is a global full-service CRO with a strong focus on quality, professional development, and supportive culture. As a client-facing role, we are looking for confident candidates with the ability to work independently whilst establishing a high-trust environment with the client’s counterparts.

Main Job Tasks and Responsibilities:

  • Responsible for protocol development including study design, sample size calculation, randomization, and statistical analysis plan for assigned studies.
  • Provide statistical oversight to studies and assure adequate quality and consistency with project requirements.
  • Responsible for assuring that data for statistical analyses are complete, accurate and consistent.
  • Responsible for statistical analysis plans and the accuracy and timeliness of statistical input into reports or decisions.
  • Responsible for validity of analysis and explore alternative analysis strategies as needed.
  • Demonstrates extensive understanding of statistical concepts and methodologies. Recognizes and corrects flaws in scientific reasoning and statistical interpretation.
  • Responsible for accuracy and consistency of statistical tables, figures, and data listings, accuracy of report text, and consistency between summary tables in the body of reports and the corresponding source tables and listings.
  • Responsible for statistical methods section for the reports. Identifies and corrects common flaws in interpretation of results, inconsistency in presentation or inference, adherence to the report guidelines, and assures project-wide consistency.
  • Effectively mentor peers with regards to statistical methodology and provide appropriate training to less experienced statisticians.
  • Manage activities of statisticians across projects by appropriately coordinating assignments and reviewing work so that projects are delivered on time with high quality.

Education and Experience:

  • MS or PhD in Statistics, Biostatistics or related field. PhD with 4-5 years of experience or MS with 7-8 years of experience.
  • Strong oral and written communications skills, with ability to effectively communicate internally and with clients.
  • Demonstrated understanding and insight in statistics, drug development process and relevant FDA regulations.
  • Pharmaceutical, CRO, or related industry experience with clinical trials, including interaction with Regulatory Agencies, especially FDA.

The Application Process

Once you have submitted your CV, you will receive an acknowledgement that we received it. If you have the requirements we need, you will be invited for phone interview as the first step. Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful.

Who will you be working for?

About ClinChoice

ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. We have over 28 years of proven high-quality delivery and results across all our services, with over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific.

Our Company Ethos

Our mission drives our culture: to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices. Our employees are the most valuable company asset and they are the fulcrum around which all ClinChoice activities are built and close management and training is the core instrument to develop and maintain highly-qualified personnel. The continuous training keeps the resources qualified in terms of competence and expertise and gives all personnel the clear tools needed to manage both internal and client processes with the same methodology. The success of these core values is evidenced by our below industry average turnover rates.

ClinChoice is an equal opportunity employer. We have based our success on attracting, developing, and promoting talent guided by diversity and inclusivity. Our employees come from very diverse backgrounds: gender, race, beliefs, and ethnicities. We recognize this is our strength and celebrate it.

#Senior #Contract

Seniority level

  • Seniority level

    Mid-Senior level

Employment type

  • Employment type

    Contract

Job function

  • Job function

    Research, Analyst, and Information Technology

  • Industries

    Pharmaceutical Manufacturing

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#699-Principal/ Senior Statistician Consultant- Late Phase Oncology (Remote in EU/UK) employer: ClinChoice

ClinChoice is an exceptional employer that prioritises professional development and a supportive work culture, making it an ideal place for Senior/Principal Statistician Consultants in Late Phase Oncology. With a commitment to quality and a diverse workforce, employees benefit from continuous training and mentorship opportunities, ensuring they are well-equipped to excel in their roles while contributing to meaningful advancements in healthcare. The remote working flexibility across the EU/UK allows for a balanced work-life integration, enhancing job satisfaction and productivity.
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Contact Detail:

ClinChoice Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land #699-Principal/ Senior Statistician Consultant- Late Phase Oncology (Remote in EU/UK)

✨Tip Number 1

Familiarise yourself with the latest statistical methodologies and software used in oncology research. Being well-versed in tools like R or SAS can set you apart, especially since this role requires a strong understanding of statistical analysis plans.

✨Tip Number 2

Network with professionals in the clinical research field, particularly those who work in oncology. Attend relevant conferences or webinars to connect with potential colleagues and learn more about the industry trends that could benefit your application.

✨Tip Number 3

Prepare to discuss your experience with regulatory agencies, especially the FDA. Highlight any past interactions you've had and how they relate to statistical oversight in clinical trials, as this is a key aspect of the role.

✨Tip Number 4

Showcase your mentoring skills during interviews. Since the role involves managing and training less experienced statisticians, be ready to share examples of how you've successfully guided others in your previous positions.

We think you need these skills to ace #699-Principal/ Senior Statistician Consultant- Late Phase Oncology (Remote in EU/UK)

Statistical Analysis
Protocol Development
Sample Size Calculation
Randomisation Techniques
Statistical Oversight
Data Quality Assurance
Statistical Analysis Plans (SAP)
Statistical Methodologies
Scientific Reasoning
Statistical Interpretation
Mentoring and Training
Project Coordination
Communication Skills
Understanding of FDA Regulations
Clinical Trial Experience

Some tips for your application 🫡

Tailor Your CV: Make sure your CV highlights relevant experience in statistics, biostatistics, and clinical trials. Emphasise your skills in protocol development, statistical analysis plans, and any experience with FDA regulations.

Craft a Strong Cover Letter: Write a cover letter that showcases your understanding of the role and the company. Mention your ability to work independently and establish trust with clients, as well as your mentoring experience with peers.

Highlight Relevant Experience: In your application, clearly outline your educational background (MS or PhD) and years of experience in the field. Include specific examples of projects where you provided statistical oversight or developed statistical methods.

Proofread Your Application: Before submitting, carefully proofread your CV and cover letter for any errors. Ensure that your documents are clear, concise, and free from inconsistencies, as attention to detail is crucial in this role.

How to prepare for a job interview at ClinChoice

✨Showcase Your Statistical Expertise

Be prepared to discuss your understanding of statistical concepts and methodologies in detail. Highlight specific examples from your past experience where you successfully applied these concepts, especially in the context of clinical trials.

✨Demonstrate Client-Facing Skills

Since this role involves direct interaction with clients, practice articulating how you've built trust and rapport in previous roles. Share anecdotes that illustrate your ability to communicate complex statistical information clearly and effectively.

✨Prepare for Technical Questions

Expect questions related to protocol development, sample size calculations, and statistical analysis plans. Brush up on these topics and be ready to explain your thought process and decision-making in past projects.

✨Emphasise Mentorship Experience

If you have experience mentoring less experienced statisticians, be sure to highlight this during the interview. Discuss how you’ve contributed to their professional development and the impact it had on project outcomes.

#699-Principal/ Senior Statistician Consultant- Late Phase Oncology (Remote in EU/UK)
ClinChoice

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  • #699-Principal/ Senior Statistician Consultant- Late Phase Oncology (Remote in EU/UK)

    Full-Time
    42000 - 84000 £ / year (est.)

    Application deadline: 2027-08-01

  • C

    ClinChoice

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