This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Senior Statistician (SAS & R) based in India.
This role offers the opportunity to apply advanced statistical expertise to support impactful clinical research and data-driven decision-making.
You will contribute to the analysis, interpretation, and reporting of clinical trial data using industry-standard statistical tools.
The position requires close collaboration with clinical, programming, and cross-functional teams to deliver accurate and meaningful insights.
You will help transform complex datasets into reliable evidence that supports research outcomes and business decisions.
This is an ideal opportunity for an experienced statistician who enjoys solving analytical challenges in a collaborative environment.
You will work on long-term projects where your expertise in SAS, R, and statistical modeling will directly contribute to successful clinical development initiatives.
Accountabilities:
As a Senior Statistician, you will lead statistical analysis activities for clinical trial programs, ensuring data accuracy, scientific rigor, and clear reporting. You will collaborate with multidisciplinary teams to interpret results, support decision-making, and deliver high-quality statistical outputs.
- Perform statistical analysis and reporting activities for clinical trial data.
- Develop and apply statistical models using SAS and R to support efficacy analysis and data interpretation.
- Analyze complex datasets and generate meaningful insights to support clinical research objectives.
- Collaborate with clinical, programming, and other cross-functional teams throughout study activities.
- Support the development of statistical reports, documentation, and analysis deliverables.
- Ensure statistical methods and outputs meet project requirements and quality standards.
- Communicate findings clearly to technical and non-technical stakeholders.
- Contribute to process improvements and effective collaboration within project teams.
- Apply best practices in statistical programming, modeling, and clinical data analysis.
Requirements:
The ideal candidate is an experienced statistician with strong expertise in clinical trial analysis and statistical programming. You should have hands-on experience with SAS and R, excellent analytical skills, and the ability to collaborate effectively with diverse teams.
- Proven experience performing statistical analysis and reporting for clinical trials.
- Strong hands-on expertise with SAS and R for statistical modeling, efficacy analysis, and data interpretation.
- Experience working closely with clinical and programming teams.
- Strong understanding of statistical methodologies used in clinical research.
- Ability to analyze, interpret, and communicate complex data findings effectively.
- Excellent documentation and reporting skills.
- Strong written and verbal communication abilities.
- Ability to work independently while collaborating effectively in a remote environment.
- Experience working in an Agile setup is preferred.
- Strong attention to detail and commitment to delivering high-quality analytical work.
Benefits:
- Long-term remote contract opportunity.
- Flexible remote work environment.
- Opportunity to contribute to meaningful clinical research initiatives.
- Competitive compensation based on experience and expertise.
- Exposure to complex statistical analysis and data-driven projects.
- Opportunity to collaborate with experienced professionals across clinical and technical teams.
- Flexible working environment supporting independent work and collaboration.
Your email job alert is now active!
