Astrazeneca
Healthcare
StatisticalProgrammingAssociateDirector
Neural analysis suggests this role is
optimal for Director candidates.
“Statistical Programming Associate Director at Astrazeneca. Skills: Statistical programming, Clinical development, Leadership. Lead project delivery. Lead technical project”
What You'll Achieve.
Deliver programming with quality; Deliver programming with timeliness
Industry & Context.
Problem solving; Troubleshooting
Onsite 3 days office/2 days home
What They're Looking For.
Must Have
Degree in Mathematics, Statistics, Computer Science, Life Science, or equivalent, Excellent programming skills in SAS (or R) and SAS macros, Thorough knowledge of the clinical development process, Thorough knowledge of industry standards (CDISC), Current knowledge of technical and regulatory requirements, Ability to proactively manage concurrent activities, Proficient ability to influence relevant stakeholders, Ability to manage risk in complicated or novel situations, Project Mindset
Nice to Have
Broad experience across multiple therapeutic areas, Experience across all phases of clinical trials, Experience in regulatory submissions, Experience in regulatory interactions
What You'll Do.
Lead project delivery
Lead technical project
Lead implementation of programming aspects
Ensure high quality of deliverables
Hold partners accountable for quality
Act as technical subject matter expert
Lead process improvement initiative
Contribute to process improvement initiative
Drive development of best practices
Drive standards development
Drive standards implementation
Manage risk in novel situations
Provide programming expertise
Provide tactical inputs
Drive ideas for improvement
Identify opportunities to improve methodology
Provide practical solutions
Manage external partners activities
Influence stakeholders on programming items
Ensure compliance to standards
Ensure automation usage
Employ project management practices
Provide input to capacity management
Maintain expertise of industry requirements
Maintain expertise of regulatory requirements
How You'll Work.
Team & Collaboration
Cross-functional teams; Global team
Communication Scope
Subject matter expertise
Process & Methodology
Project management practices
Full Job Description
**Role Barcelona onsite 3 days office/2 days home** Would you like to be part of a fast-paced and agile global team that has direct strategic impact on drug development, empowered and trusted to innovate and experiment? Join us at AstraZeneca CVRM (Cardiovascular Renal Metabolism) Biometrics to impact a wide range of engaging projects striving to make a difference for millions of patients. Our Biometrics team consists of Statisticians, Statistical Programmers, Information and Data Scientists. We drive and contribute to optimized clinical drug development programs and access to information and scientific knowledge management. We are now offering an exciting opportunity for a dedicated and highly motivated individual to join us as **Statistical Programming Associate Director. ** This role is a delivery focused technical leadership role for programming and overseeing deliverables with quality and timeliness, following established standards and processes. This leadership role requires profound programming experience and excellent industry knowledge to independently lead implementation of programming activities and guide other programmers. You will provide subject matter expertise within the Programming discipline and act as a specialist within cross-functional teams to deliver continuous improvement. This role will be placed at AstraZeneca’s dynamic R&D global hub in Barcelona (Spain), where you will work in an international environment at the forefront of clinical development. **Accountabilities:** As a Statistical Programming Associate Director, you are responsible for leading and directing the full scope of project delivery and/or lead a technical project within the TA/Drug Project/Study/Function. Typical accountabilities include: * Leading implementation of statistical programming aspects of the protocol or clinical development program * Responsible for the high quality of all project deliverables, holding partners, and providers accountable for the quality of their
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