Biostatistician

RemoteJobsOne; Brussel; À distance; EUR 73 000 - 122 000; Temps partiel

Résumé du poste

RemoteJobsOne is seeking a Biostatistician for a fully remote contractor role based in Belgium. You will apply your domain expertise to train next-generation AI systems by designing expert-level evaluation tasks, sourcing real-world datasets, and defining rigorous methodological solutions for each scenario.

This role emphasizes regulatory-ready analysis, high-quality documentation, and collaboration with stakeholders to ensure compliance with standards.

Qualifications

• MS or PhD in biostatistics, statistics, or epidemiology.
• 4+ years of experience in pharmaceutical, contract research, hospital, or academic medical contexts.
• Demonstrated command of clinical study design, regulatory documentation, and observational research methodologies.
• Advanced proficiency in R, Python, SAS, or Stata applied to real clinical or epidemiological datasets.
• Strong attention to methodological detail, clinical interpretation, and regulatory sensitivity.
• Experience preparing submission-ready deliverables for regulatory agencies (e.g., FDA, EMA) is a plus.
• Excellent written communication skills and ability to author detailed grading rubrics and technical documentation.

Responsabilités

• Design and author expert-level evaluation tasks simulating real-world biostatistics challenges.
• Source, construct, and curate authentic datasets for task use.
• Define correct methodological solutions and defensible clinical interpretations for evaluation scenarios.
• Develop comprehensive, 35+ item rubrics to evaluate AI agent performance with respect to methodological rigor and clinical reasoning.
• Ensure all tasks reflect the complexity and depth of real-world biostatistics practice, avoiding simplified or textbook-style examples.
• Collaborate with project stakeholders to ensure deliverables align with regulatory and scientific standards.

Connaissances

Clinical study design

Regulatory documentation

Observational research methodologies

Written communication

Regulatory submissions

Formation

MS/PhD in biostatistics or epidemiology

Outils

R

Python

SAS

Stata

Description du poste

IMPORTANT: after you apply, please check your email. We send you a link to complete your application — it is not considered until that last step is done. If you do not see it, check your spam folder.

This is a fully remote position, open to candidates based in Belgium.

Pay: $60–$100/hr

Role Title: Biostatistician

Role Type: Contractor

Location: Remote

We are engaging Biostatisticians to contribute to a customer's advanced project in AI benchmarking. In this role, you'll apply your expertise to help train next-generation AI systems. Your work will shape how models learn, reason, and perform through high-quality, real-world input. No prior experience in AI is required — your domain knowledge is what matters.

Scope of Work

1. Design and author expert-level evaluation tasks simulating real-world biostatistics challenges, such as clinical trial analysis, regulatory submission reviews, and observational study assessments.
2. Source, construct, and curate authentic datasets including trial data, patient records, and protocol documents for task use.
3. Define correct methodological solutions and defensible clinical interpretations for each evaluation scenario.
4. Develop comprehensive, 35+ item rubrics to evaluate AI agent performance with respect to methodological rigor and clinical reasoning.
5. Ensure all tasks reflect the complexity and depth of real-world biostatistics practice, avoiding simplified or textbook-style examples.
6. Collaborate with project stakeholders to ensure deliverables align with regulatory and scientific standards.

Preferred Qualifications

1. MS or PhD in biostatistics, statistics, or epidemiology.
2. 4+ years of experience in pharmaceutical, contract research, hospital, or academic medical contexts.
3. Demonstrated command of clinical study design, regulatory documentation, and observational research methodologies.
4. Advanced proficiency in R, Python, SAS, or Stata applied to real clinical or epidemiological datasets.
5. Strong attention to methodological detail, clinical interpretation, and regulatory sensitivity.
6. Experience preparing submission-ready deliverables for regulatory agencies (e.g., FDA, EMA) is a plus.
7. Excellent written communication skills and ability to author detailed grading rubrics and technical documentation.

Compensation Structure

Compensation is output-based; experts are paid per task that meets the project specifications. The time required to complete work may vary depending on the expert’s experience and workflow. Minimum submission requirements apply. Experts must submit a minimum of tasks per week.

Start Timeline & Availability

We typically fill roles within 48 hours and are looking for experts ready to jump in right away. If selected, we expect you to start your first tasks within 24–48 hours of completing onboarding.