Responsibilities
- Develop and maintain statistical analysis plans and programs.
- Ensure data integrity and accuracy in clinical trials.
- Collaborate with cross-functional teams to deliver high-quality data analysis.
- Provide statistical expertise and support to clinical trial projects.
- Generate and interpret statistical reports and visualizations.
- Conduct data validation and quality control checks.
- Assist in the preparation of regulatory submissions.
- Stay updated with industry standards and best practices in statistical programming.
- Contribute to the development and improvement of statistical programming standards and procedures.
- Participate in project meetings and provide updates on statistical analysis progress.
- Troubleshoot and resolve statistical programming issues.
- Document statistical analysis methods and results.
- Review and validate statistical analysis outputs.
- Provide training and mentorship to junior team members.
- Ensure compliance with regulatory requirements and guidelines.
- Support the development of statistical models and algorithms.
- Conduct statistical analysis for various clinical trial phases.
- Collaborate with data management teams to ensure data consistency.
- Develop and implement statistical programming solutions.
- Review and approve statistical analysis plans and programs.
- Participate in the development of statistical programming tools and software.
- Provide statistical support for clinical trial protocols and study designs.
- Ensure timely delivery of statistical analysis outputs.
Nice to Have
- Experience with clinical trial data and regulatory requirements.
- Knowledge of statistical methods and techniques used in clinical research.
- Experience with data management and validation processes.
- Familiarity with clinical trial protocols and study designs.
- Knowledge of regulatory guidelines and standards.
- Experience with statistical modeling and algorithm development.
- Familiarity with clinical trial data standards and formats.
- Experience with statistical analysis for various clinical trial phases.
- Knowledge of statistical programming best practices and standards.
- Experience with regulatory submissions and documentation.
- Familiarity with clinical trial data management systems.
- Experience with statistical analysis for clinical trial protocols and study designs.
Work Arrangement
Outside IR35
Team
Part of a team of statisticians and programmers.
About the Role
- This role involves working on clinical trials and data analysis, focusing on statistical programming and analysis.
- The ideal candidate will have experience in the pharmaceutical or biotechnology industry and be proficient in statistical programming languages such as SAS, R, or Python.
- The role requires strong analytical and problem-solving skills, as well as the ability to work independently and as part of a team.
- The candidate will be responsible for developing and maintaining statistical analysis plans and programs, ensuring data integrity and accuracy in clinical trials, and collaborating with cross-functional teams to deliver high-quality data analysis.
- The role also involves providing statistical expertise and support to clinical trial projects, generating and interpreting statistical reports and visualizations, and conducting data validation and quality control checks.
- The candidate will assist in the preparation of regulatory submissions, stay updated with industry standards and best practices in statistical programming, and contribute to the development and improvement of statistical programming standards and procedures.
- The role requires participation in project meetings, providing updates on statistical analysis progress, troubleshooting and resolving statistical programming issues, and documenting statistical analysis methods and results.
- The candidate will review and validate statistical analysis outputs, provide training and mentorship to junior team members, and ensure compliance with regulatory requirements and guidelines.
- The role also involves supporting the development of statistical models and algorithms, conducting statistical analysis for various clinical trial phases, and collaborating with data management teams to ensure data consistency.
- The candidate will develop and implement statistical programming solutions, review and approve statistical analysis plans and programs, and participate in the development of statistical programming tools and software.
What We Offer
- Competitive compensation and benefits package.
- Flexible work arrangements and remote work options.
- Opportunities for professional development and growth.
- Collaborative and supportive work environment.
- Challenging and rewarding projects in the pharmaceutical industry.
- Access to state-of-the-art tools and technologies.
- Supportive team and management.
- Opportunities for training and skill development.
- Competitive compensation and benefits package.
- Flexible work arrangements and remote work options.
- Opportunities for professional development and growth.
- Collaborative and supportive work environment.
- Challenging and rewarding projects in the pharmaceutical industry.
- Access to state-of-the-art tools and technologies.
- Supportive team and management.
- Opportunities for training and skill development.
How to Apply
- Interested candidates are encouraged to submit their resume and cover letter for consideration.
- Please include relevant experience and qualifications in your application.
- Applications will be reviewed on a rolling basis, so early submission is encouraged.
- Only shortlisted candidates will be contacted for an interview.
- The application process may include a technical assessment and behavioral interview.
- Candidates must be eligible to work in the UK and be able to work remotely.
- Interested candidates are encouraged to submit their resume and cover letter for consideration.
- Please include relevant experience and qualifications in your application.
- Applications will be reviewed on a rolling basis, so early submission is encouraged.
- Only shortlisted candidates will be contacted for an interview.
- The application process may include a technical assessment and behavioral interview.
- Candidates must be eligible to work in the UK and be able to work remotely.
Not provided
