REMOTE Principal Statistician- (Clinical) - UK

Are you interested in working directly for a single sponsor while enjoying the security and career opportunities offered by a global CRO? Our team believes it's the best of both worlds.

ClinChoice is seeking a Principal Statistician to join our biometrics team. This is a full-time, permanent position with REMOTE options available in the UK and Italy.

ClinChoice is a global full-service CRO emphasizing quality, professional development, and a supportive culture. We are hiring a Principal Statistician responsible for protocol development and statistical analysis plans for assigned studies. Additional responsibilities include providing statistical oversight to ensure quality and consistency with project requirements.

Job Responsibilities

1. Develop protocols including study design, sample size calculation, randomization, and statistical analysis plans.
2. Oversee statistical aspects of studies to ensure quality and adherence to project requirements.
3. Ensure data used in analyses are complete, accurate, and consistent.
4. Prepare statistical analysis plans and ensure timely and accurate statistical input into reports and decisions.
5. Validate analysis methods and explore alternative strategies as needed.
6. Demonstrate extensive understanding of statistical concepts and methodologies, identifying and correcting flaws in scientific reasoning and interpretation.
7. Ensure accuracy and consistency of statistical tables, figures, data listings, and report text, maintaining alignment between summaries and source data.
8. Draft the statistical methods section of reports, correcting common flaws and ensuring project-wide consistency.
9. Mentor peers on statistical methodologies and provide training to less experienced statisticians.
10. Manage activities of statisticians across projects, coordinating assignments and reviewing work to ensure timely, high-quality delivery.

Requirements

• MS or PhD in Statistics, Biostatistics, or a related field. PhD with 3-5 years of experience or MS with 7-8 years of experience.
• Strong communication skills, both oral and written, for effective interaction internally and with clients.
• Solid understanding of statistics, drug development processes, and FDA regulations.
• Experience in the pharmaceutical or CRO industry with clinical trials, including interaction with regulatory agencies such as the FDA.

The Application Process

After submitting your CV, you will receive acknowledgment of receipt. If you meet the requirements, you will be invited for a phone interview. Due to high application volume, we may not respond individually to unsuccessful candidates.

About ClinChoice

ClinChoice is a global full-service CRO specializing in clinical development for pharmaceutical, biotech, medical device, and consumer health companies. With over 28 years of experience and more than 4,000 professionals across 20+ countries, we deliver high-quality results worldwide.

Our Ethos

Our mission is to contribute to a healthier, safer world by accelerating the development and commercialization of innovative drugs and devices. We value our employees highly, fostering a culture of continuous training and development, which reflects in our low turnover rates.

ClinChoice is committed to diversity and inclusion, celebrating the varied backgrounds of our staff. We are an equal opportunity employer.

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