Biostatistician

GluCare

Dubai

On-site

AED 300,000 - 540,000

Full time

14 days+
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Job summary

GluCare Integrated Diabetes Center in Dubai seeks a highly skilled Biostatistician to support clinical research and data analytics, designing experiments and guiding data-driven decisions across healthcare and research teams.

You will analyze clinical data, contribute to trial design and modeling, collaborate with clinicians and IT, and translate complex results into actionable insights while ensuring regulatory compliance.

Qualifications

  • Masters or PhD in Biostatistics or related field.
  • Experience as a Biostatistician in clinical/healthcare.
  • Proficiency in SAS, R, SPSS or Stata.
  • Strong understanding of trial design, epidemiology and data modeling.
  • Excellent problem-solving and communication skills.
  • Knowledge of HIPAA and GDPR is a plus.

Responsibilities

  • Data Analysis: Perform statistical analyses on clinical data including patient outcomes and intervention effects.
  • Study Design: Design studies including randomized trials and observational studies.
  • Data Interpretation: Provide insights and actionable recommendations from data.
  • Model Development: Develop statistical models to support decision-making and prediction.
  • Collaboration: Work with clinicians, researchers and IT teams for data collection and analysis.
  • Reporting: Prepare reports and presentations to communicate findings to teams and leadership.
  • Compliance: Ensure compliance with regulatory requirements for clinical trials and research.
  • Continuous Improvement: Improve data collection and analysis tools for data quality.

Skills

Data analysis
Study design
Data modeling
Collaboration
Communication
Regulatory compliance
Problem solving

Education

Master's or PhD in Biostatistics or related field

Tools

SAS
R
SPSS
Stata

Job description

Job Summary: GluCare Integrated Diabetes Center is seeking a highly skilled Biostatistician to support our clinical research and data analytics efforts. The ideal candidate will work closely with our healthcare and research teams to analyze patient data design experiments and contribute to data-driven decision-making processes. This role is critical in advancing our mission to improve diabetes care through innovation and technology.

Key Responsibilities:

  • Data Analysis: Perform statistical analyses on clinical data including patient outcomes intervention effects and epidemiological studies.
  • Study Design: Collaborate with clinical researchers to design studies including randomized controlled trials and observational studies ensuring statistical rigor.
  • Data Interpretation: Provide insights and actionable recommendations based on data and assist in the interpretation of statistical findings.
  • Model Development: Develop and apply statistical models to support clinical decision-making and predictive analysis.
  • Collaboration: Work closely with clinicians researchers and IT teams to ensure accurate data collection integration and analysis.
  • Reporting: Prepare reports charts and presentations to communicate statistical findings to clinical teams stakeholders and leadership.
  • Compliance: Ensure compliance with regulatory requirements for clinical trials and research including ethical standards and data privacy regulations.
  • Continuous Improvement: Contribute to the development of data collection and analysis tools ensuring continuous improvements in data quality and usability.

Requirements

  • Masters or PhD in Biostatistics Statistics or a related field.
  • Proven experience as a Biostatistician in a clinical or healthcare setting preferably in diabetes or chronic disease management.
  • Proficiency in statistical software such as SAS R SPSS or Stata.
  • Strong understanding of clinical trial design epidemiology and data modeling.
  • Excellent problem-solving skills with the ability to translate complex data into actionable insights.
  • Strong communication skills with the ability to collaborate effectively with both technical and non-technical teams.
  • Knowledge of healthcare data standards and regulations including HIPAA and GDPR is a plus.

Required Experience:

IC

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