Assoc Director, Statistical Programming
Novartis
Assoc Director, Statistical Programming
Job Description
Summary
Summary The Early Development, Associate Director, Statistical Programming , is responsible for all statistical programming aspects of one or more drug development programs or indication programs with Early Development space.As a program lead, the Associate Director ensures cross-functional collaboration within and outside AQS and decision-making for assigned trials/programs in drug life cycle management. They ensure that the assigned trials/programs are adequately resourced, and oversee all aspects of programming, quality and regulatory compliance.
This key leadership position ensures the efficient execution of trial/program level plans, delivering high-quality results on time. A thorough understanding of the drug development process, experience in regulatory activities, and expertise in statistical reporting, along with a proven track record in operational or functional leadership, is required.
Locations
- United Kingdom
Salary
Estimated Salary Rangemedium confidence
80,000 - 135,000 GBP / yearly
* This is an estimated range based on market data and may vary based on experience and qualifications.
Skills Required
- Statistical programmingintermediate
- Drug development processintermediate
- Regulatory complianceintermediate
- Cross-functional collaborationintermediate
- Quality managementintermediate
- Leadershipintermediate
- Program managementintermediate
- Statistical reportingintermediate
Required Qualifications
- Associate Director experience in statistical programming (experience)
- Experience in early drug development (experience)
- Proven track record in operational or functional leadership (experience)
- Expertise in regulatory activities (experience)
Responsibilities
- Handle all statistical programming aspects for drug development programs
- Ensure cross-functional collaboration within and outside AQS
- Make decisions for assigned trials/programs in drug lifecycle management
- Ensure trials/programs are adequately resourced
- Oversee programming, quality, and regulatory compliance
- Execute trial/program level plans delivering high-quality results on time
Answer 10 quick questions to check your fit for Assoc Director, Statistical Programming @ Novartis.
10 Questions
~2 Minutes
Instant Score
Assoc Director, Statistical Programming
Novartis
Assoc Director, Statistical Programming
Job Description
Summary
Summary The Early Development, Associate Director, Statistical Programming , is responsible for all statistical programming aspects of one or more drug development programs or indication programs with Early Development space.As a program lead, the Associate Director ensures cross-functional collaboration within and outside AQS and decision-making for assigned trials/programs in drug life cycle management. They ensure that the assigned trials/programs are adequately resourced, and oversee all aspects of programming, quality and regulatory compliance.
This key leadership position ensures the efficient execution of trial/program level plans, delivering high-quality results on time. A thorough understanding of the drug development process, experience in regulatory activities, and expertise in statistical reporting, along with a proven track record in operational or functional leadership, is required.
Locations
- United Kingdom
Salary
Estimated Salary Rangemedium confidence
80,000 - 135,000 GBP / yearly
* This is an estimated range based on market data and may vary based on experience and qualifications.
Skills Required
- Statistical programmingintermediate
- Drug development processintermediate
- Regulatory complianceintermediate
- Cross-functional collaborationintermediate
- Quality managementintermediate
- Leadershipintermediate
- Program managementintermediate
- Statistical reportingintermediate
Required Qualifications
- Associate Director experience in statistical programming (experience)
- Experience in early drug development (experience)
- Proven track record in operational or functional leadership (experience)
- Expertise in regulatory activities (experience)
Responsibilities
- Handle all statistical programming aspects for drug development programs
- Ensure cross-functional collaboration within and outside AQS
- Make decisions for assigned trials/programs in drug lifecycle management
- Ensure trials/programs are adequately resourced
- Oversee programming, quality, and regulatory compliance
- Execute trial/program level plans delivering high-quality results on time
Answer 10 quick questions to check your fit for Assoc Director, Statistical Programming @ Novartis.
10 Questions
~2 Minutes
Instant Score