Senior Clinical Systems Analyst
Bristol-Myers Squibb
Senior Clinical Systems Analyst
Job Description
Executes the protocol simplification objectives across multiple therapeutic areas. Sets priorities for the team to ensure task completion and connectivity to clinical protocol process. Drive process improvements and technology enhancements in partnership with IT and other teams. Ensure alignment of clinical study design with quality-by-design principles. Build and maintain a digital document management system for accurate logging, tracking, and secure archiving of workshop materials. Lead workshops and guide teams in using supporting platforms effectively. Operate independently while fostering collaboration in a matrixed environment. Develop key performance indicators (KPIs) to measure protocol simplification success. Monitor, analyze, and report on metrics such as review turnaround times and workload distribution. Lead road-shows and training sessions to ensure consistent messaging and adoption. Provide timely updates and status reports to management. Prepare and distribute training materials, guidance documents, and stakeholder communications. Support audit and inspection readiness through document retrieval and coordination. Supporting People with Disabilities Bachelor's degree in life sciences, healthcare, business administration, or related field 3-5 years (minimum) of experience in clinical research, biopharma, or a regulated industry Conceptual and practical expertise in own discipline and basic knowledge of related disciplines Innovative mindset with a passion for leveraging technology to improve processes Proven commitment to quality, compliance, and continuous improvement Strong organizational and time management skills, with attention to detail Proficiency with Microsoft Office, document management systems, AI, and other data analytic tools Demonstrated commitment to quality, compliance, and process improvement Ability to work collaboratively and adapt in a fast-paced environment
About the Role/Company
- Supporting People with Disabilities
Key Responsibilities
- Execute protocol simplification objectives across multiple therapeutic areas
- Set priorities for the team to ensure task completion and connectivity to clinical protocol process
- Drive process improvements and technology enhancements in partnership with IT and other teams
- Ensure alignment of clinical study design with quality-by-design principles
- Build and maintain a digital document management system for accurate logging, tracking, and secure archiving of workshop materials
- Lead workshops and guide teams in using supporting platforms effectively
- Operate independently while fostering collaboration in a matrixed environment
- Develop key performance indicators (KPIs) to measure protocol simplification success
- Monitor, analyze, and report on metrics such as review turnaround times and workload distribution
- Lead road-shows and training sessions to ensure consistent messaging and adoption
- Provide timely updates and status reports to management
- Prepare and distribute training materials, guidance documents, and stakeholder communications
- Support audit and inspection readiness through document retrieval and coordination
Required Qualifications
- Bachelor's degree in life sciences, healthcare, business administration, or related field
- -5 years (minimum) of experience in clinical research, biopharma, or a regulated industry
Skills Required
- Conceptual and practical expertise in own discipline and basic knowledge of related disciplines
- Innovative mindset with a passion for leveraging technology to improve processes
- Proven commitment to quality, compliance, and continuous improvement
- Strong organizational and time management skills, with attention to detail
- Proficiency with Microsoft Office, document management systems, AI, and other data analytic tools
- Demonstrated commitment to quality, compliance, and process improvement
- Ability to work collaboratively and adapt in a fast-paced environment
Locations
- Warsaw, PL
Salary
Salary not disclosed
Estimated Salary Rangemedium confidence
120,000 - 180,000 PLN / yearly
Source: ai estimated
* This is an estimated range based on market data and may vary based on experience and qualifications.
Skills Required
- Conceptual and practical expertise in own discipline and basic knowledge of related disciplinesintermediate
- Innovative mindset with a passion for leveraging technology to improve processesintermediate
- Proven commitment to quality, compliance, and continuous improvementintermediate
- Strong organizational and time management skills, with attention to detailintermediate
- Proficiency with Microsoft Office, document management systems, AI, and other data analytic toolsintermediate
- Demonstrated commitment to quality, compliance, and process improvementintermediate
- Ability to work collaboratively and adapt in a fast-paced environmentintermediate
Required Qualifications
- Bachelor's degree in life sciences, healthcare, business administration, or related field (experience)
- -5 years (minimum) of experience in clinical research, biopharma, or a regulated industry (experience)
Responsibilities
- Execute protocol simplification objectives across multiple therapeutic areas
- Set priorities for the team to ensure task completion and connectivity to clinical protocol process
- Drive process improvements and technology enhancements in partnership with IT and other teams
- Ensure alignment of clinical study design with quality-by-design principles
- Build and maintain a digital document management system for accurate logging, tracking, and secure archiving of workshop materials
- Lead workshops and guide teams in using supporting platforms effectively
- Operate independently while fostering collaboration in a matrixed environment
- Develop key performance indicators (KPIs) to measure protocol simplification success
- Monitor, analyze, and report on metrics such as review turnaround times and workload distribution
- Lead road-shows and training sessions to ensure consistent messaging and adoption
- Provide timely updates and status reports to management
- Prepare and distribute training materials, guidance documents, and stakeholder communications
- Support audit and inspection readiness through document retrieval and coordination
Tags & Categories
Senior Clinical Systems Analyst
Bristol-Myers Squibb
Senior Clinical Systems Analyst
Job Description
Executes the protocol simplification objectives across multiple therapeutic areas. Sets priorities for the team to ensure task completion and connectivity to clinical protocol process. Drive process improvements and technology enhancements in partnership with IT and other teams. Ensure alignment of clinical study design with quality-by-design principles. Build and maintain a digital document management system for accurate logging, tracking, and secure archiving of workshop materials. Lead workshops and guide teams in using supporting platforms effectively. Operate independently while fostering collaboration in a matrixed environment. Develop key performance indicators (KPIs) to measure protocol simplification success. Monitor, analyze, and report on metrics such as review turnaround times and workload distribution. Lead road-shows and training sessions to ensure consistent messaging and adoption. Provide timely updates and status reports to management. Prepare and distribute training materials, guidance documents, and stakeholder communications. Support audit and inspection readiness through document retrieval and coordination. Supporting People with Disabilities Bachelor's degree in life sciences, healthcare, business administration, or related field 3-5 years (minimum) of experience in clinical research, biopharma, or a regulated industry Conceptual and practical expertise in own discipline and basic knowledge of related disciplines Innovative mindset with a passion for leveraging technology to improve processes Proven commitment to quality, compliance, and continuous improvement Strong organizational and time management skills, with attention to detail Proficiency with Microsoft Office, document management systems, AI, and other data analytic tools Demonstrated commitment to quality, compliance, and process improvement Ability to work collaboratively and adapt in a fast-paced environment
About the Role/Company
- Supporting People with Disabilities
Key Responsibilities
- Execute protocol simplification objectives across multiple therapeutic areas
- Set priorities for the team to ensure task completion and connectivity to clinical protocol process
- Drive process improvements and technology enhancements in partnership with IT and other teams
- Ensure alignment of clinical study design with quality-by-design principles
- Build and maintain a digital document management system for accurate logging, tracking, and secure archiving of workshop materials
- Lead workshops and guide teams in using supporting platforms effectively
- Operate independently while fostering collaboration in a matrixed environment
- Develop key performance indicators (KPIs) to measure protocol simplification success
- Monitor, analyze, and report on metrics such as review turnaround times and workload distribution
- Lead road-shows and training sessions to ensure consistent messaging and adoption
- Provide timely updates and status reports to management
- Prepare and distribute training materials, guidance documents, and stakeholder communications
- Support audit and inspection readiness through document retrieval and coordination
Required Qualifications
- Bachelor's degree in life sciences, healthcare, business administration, or related field
- -5 years (minimum) of experience in clinical research, biopharma, or a regulated industry
Skills Required
- Conceptual and practical expertise in own discipline and basic knowledge of related disciplines
- Innovative mindset with a passion for leveraging technology to improve processes
- Proven commitment to quality, compliance, and continuous improvement
- Strong organizational and time management skills, with attention to detail
- Proficiency with Microsoft Office, document management systems, AI, and other data analytic tools
- Demonstrated commitment to quality, compliance, and process improvement
- Ability to work collaboratively and adapt in a fast-paced environment
Locations
- Warsaw, PL
Salary
Salary not disclosed
Estimated Salary Rangemedium confidence
120,000 - 180,000 PLN / yearly
Source: ai estimated
* This is an estimated range based on market data and may vary based on experience and qualifications.
Skills Required
- Conceptual and practical expertise in own discipline and basic knowledge of related disciplinesintermediate
- Innovative mindset with a passion for leveraging technology to improve processesintermediate
- Proven commitment to quality, compliance, and continuous improvementintermediate
- Strong organizational and time management skills, with attention to detailintermediate
- Proficiency with Microsoft Office, document management systems, AI, and other data analytic toolsintermediate
- Demonstrated commitment to quality, compliance, and process improvementintermediate
- Ability to work collaboratively and adapt in a fast-paced environmentintermediate
Required Qualifications
- Bachelor's degree in life sciences, healthcare, business administration, or related field (experience)
- -5 years (minimum) of experience in clinical research, biopharma, or a regulated industry (experience)
Responsibilities
- Execute protocol simplification objectives across multiple therapeutic areas
- Set priorities for the team to ensure task completion and connectivity to clinical protocol process
- Drive process improvements and technology enhancements in partnership with IT and other teams
- Ensure alignment of clinical study design with quality-by-design principles
- Build and maintain a digital document management system for accurate logging, tracking, and secure archiving of workshop materials
- Lead workshops and guide teams in using supporting platforms effectively
- Operate independently while fostering collaboration in a matrixed environment
- Develop key performance indicators (KPIs) to measure protocol simplification success
- Monitor, analyze, and report on metrics such as review turnaround times and workload distribution
- Lead road-shows and training sessions to ensure consistent messaging and adoption
- Provide timely updates and status reports to management
- Prepare and distribute training materials, guidance documents, and stakeholder communications
- Support audit and inspection readiness through document retrieval and coordination
Tags & Categories