4 Biostatistician jobs in Saudi Arabia
Senior Biostatistician
Posted today
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Job Description
• Lead statistical analysis planning, execution, and interpretation for clinical studies.
• Develop and apply advanced modeling techniques, including regression modeling, survival analysis, mixed-effects models, and causal inference methods (e.g., propensity scores, inverse probability weighting).
• Design and analyze matched cohort studies and high-dimensional real-world data projects using robust epidemiologic methods.
• Collaborate with clinical teams on protocol development, study design, and data analysis and interpretation.
• Use R, Stata, and/or Python to build reproducible workflows for data cleaning, analysis, and visualization.
• Contribute to the development of risk prediction models and explore AI/ML techniques for selected research questions.
• Mentor junior biostatisticians, analysts, and data managers in best practices.
• Support manuscript and grant writing with methodological input and statistical reporting.
Required Qualifications
• Master's or PhD in Biostatistics, Epidemiology, Data Science, or a related quantitative field.
• Minimum 3–5 years of experience working in clinical or health data research.
• Experience in matched analysis, causal modeling, or longitudinal data analysis.
• Strong expertise in advanced statistical techniques (e.g., GLM, time-to-event modeling, repeated measures).
• Proficiency in at least two statistical programming environments (e.g., R, Stata, Python).
• Familiarity with large clinical datasets such as EHRs, registries, or administrative databases.
• Ability to clearly communicate technical methods and findings to diverse audiences.
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Desirable Qualifications
• Interest or applied experience in machine learning, AI, or NLP in health-related settings.
• Exposure to neural networks, decision trees, or ensemble models using Python libraries (e.g., scikit-learn, XGBoost, PyTorch).
• Familiarity with data visualization, reproducibility tools (e.g., Git, R Markdown), or pipeline development.
• Experience contributing to peer-reviewed publications or grant applications.
Data Analysis Specialist
Posted today
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Job Description
Job Description
- Collect, clean, and transform structured and unstructured datasets from multiple sources (databases, APIs, data warehouses, and flat files) for analysis.
- Develop, maintain, and optimize SQL queries, stored procedures, and ETL pipelines to ensure reliable data flows.
- Perform statistical analysis, hypothesis testing, and predictive modeling to extract actionable insights and support decision-making.
- Create advanced dashboards and reports using tools such as Power BI, Tableau, or Looker, ensuring KPIs are tracked and visualized effectively.
- Collaborate with data engineers and business stakeholders to define data requirements and ensure alignment between technical outputs and business needs.
- Apply data mining, clustering, and regression techniques to detect patterns, trends, and anomalies across large datasets.
- Document methodologies, maintain reproducibility of analysis, and adhere to best practices for version control and code management (e.g., Git).
Job Requirements
- A degree in computer science, data science or any other relevant field. A master's is a plus
- 4 years of experience in relevant fields
- Data Engineering & Querying: Strong proficiency in SQL
- Visualization & Reporting: Advanced skills in BI tools (Power BI, Tableau, Looker, or equivalent) and ability to design performance-optimized dashboards.
- Data Wrangling: Ability to handle raw, messy data—cleaning, normalizing, feature engineering, and managing large datasets with performance considerations.
- Cloud & Analytics Tools: Familiarity with cloud platforms (GCP BigQuery, AWS Redshift, Azure Synapse) and distributed data systems (Spark, Hadoop) is a plus as well as hands-on experience on Dataiku is a plus.
Clinical Trials Assistant with Finance Responsibilities
Posted today
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Job Description
Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems (e.g., Trial Master File (TMF)) that track site compliance and performance within project timelines.
Assist the clinical team with the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures.
Assist with periodic review of study files for completeness.
Assist CRAs and RSU with preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information. Coordinate the tracking and management of Case Report Forms (CRFs), queries and clinical data flow.
Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation.
May accompany CRAs on site visits to assist with clinical monitoring duties upon completion of required training.
May collaborate with the clinical team on the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures.
High School Diploma or equivalent Req
At least 1 year experience as CTA with Finance responsibilities
Experience in contracts, payments, budgeting, invoicing
Equivalent combination of education, training and experience.
Minimum one year clinical research experience strongly preferred.
Computer skills including working knowledge of Microsoft Word, Excel and PowerPoint.
Written and verbal communication skills including good command of Greek and English language.
Effective time management and organizational skills.
Ability to establish and maintain effective working relationships with coworkers, managers, and clients.
Basic knowledge of applicable clinical research regulatory requirement, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines as provided in company training.
Knowledge of applicable protocol requirements as provided in company training.
Clinical Trials Assistant with Finance Responsibilities Sponsor-dedicated
Posted 17 days ago
Job Viewed
Job Description
Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery.
**Essential Functions**
- Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems (e.g., Trial Master File (TMF)) that track site compliance and performance within project timelines.
- Assist the clinical team with the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures.
- Assist with periodic review of study files for completeness.
- Assist CRAs and RSU with preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information. Coordinate the tracking and management of Case Report Forms (CRFs), queries and clinical data flow.
- Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation.
- May accompany CRAs on site visits to assist with clinical monitoring duties upon completion of required training.
- May collaborate with the clinical team on the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures.
**Qualifications**
- High School Diploma or equivalent Req
- At least 1 year experience as CTA with Finance responsibilities
- Experience in contracts, payments, budgeting, invoicing
- Equivalent combination of education, training and experience.
- Minimum one year clinical research experience strongly preferred.
- Computer skills including working knowledge of Microsoft Word, Excel and PowerPoint.
- Written and verbal communication skills including good command of Greek and English language.
- Effective time management and organizational skills.
- Ability to establish and maintain effective working relationships with coworkers, managers, and clients.
- Basic knowledge of applicable clinical research regulatory requirement, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines as provided in company training.
- Knowledge of applicable protocol requirements as provided in company training.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
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