Skills this job asks for
StatisticsLeadershipCompliance
Add your CV (free) to see which of these your CV is missing.
Sponsorship verdict
No sponsorship evidence yet
No government record and no wording either way. Not a refusal: ask the recruiter.
-
?
No government sponsor record hereNo government sponsor record covers this employer in this country.
-
?
The posting doesn’t mention sponsorshipSilence isn’t a refusal — ask the recruiter before investing much time.
-
?
Can’t check pay against the visa rulesWe don’t have visa salary rules for this country yet.
-
✓
Confirmed live todayWhen a source last listed this job as open.
Details and sources
A verdict summarises public evidence. It is not legal advice and never a guarantee: the employer and the immigration authority decide. Sign in to factor in where you can already work.
Before you apply
Sponsorship unknown
No register record and no sponsorship wording in the posting. Worth asking the employer before investing significant time.
These come from the posting’s own wording. Read the original listing to confirm. See better-fit alternatives →
About the role
Job Title: Associate Director Statistical Programming
• Career Level – E
• Location: Manyata Tech Park, Bangalore
• Work Type: Hybrid
About AstraZeneca:
AstraZeneca is a global, science-led, patient-focused pharmaceutical company that focuses on the research, development, and commercialisation of prescription medicines. We aim to transform the lives of patients with improved outcomes and a better quality of life. But we’re more than one of the world’s leading pharmaceutical companies. At AstraZeneca, we 're dedicated to being a Great Place to Work.
Introduction to role:
Are you ready to lead a high-visibility programming team that turns complex clinical data into decisions that change outcomes for patients in cardiovascular, renal and metabolism? Do you want your expertise to be seen and heard across global studies, shaping the end deliverables that move our medicines forward?
In this senior role, you will lead and develop a team of programmers, guiding delivery across a moderate-scope drug program or multiple smaller projects. You will be the go-to expert for programming strategy, partnering closely with statisticians, clinicians and data leaders to raise standards, accelerate execution and ensure every line of code stands up to regulatory scrutiny.
Accountabilities:
• Team Leadership and Development: Lead, mentor and grow a high-performing programming team; set clear objectives, structure work for focus and collaboration, and ensure training and timesheet compliance to build enduring capability.
• Strategic Resourcing and Capacity: Translate business needs into actionable resourcing plans; provide capacity input across studies, recruit for critical skills and retain talent through targeted development.
• Program Delivery and Technical Ownership: Lead implementation of statistical programming for protocols and clinical development programs; serve as a subject matter expert for the therapy area, project or function to resolve complex issues and guide technical decisions.
• Quality, Standards and Automation: Own quality and compliance for programming deliverables, holding internal teams and external partners accountable; drive standards development, measure adherence to data standards and automation, and embed consistent practices.
• External Partnerships: Manage Contract Research Organisations and contracting staff to deliver on time, to scope and to the highest quality, calling out and mitigating risks in complicated or novel situations.
• Cross-Functional Influence and Continuous Improvement: Represent Programming leadership in cross-functional settings; influence stakeholders with clear, evidence-based recommendations; lead or contribute to process improvements, best of industry practices, training and mentorship that lift quality, efficiency and effectiveness across the function.
• Safety, Health and Environment (SHE) and Compliance: Operate in line with the agreed SHE strategy by managing risks, incidents, reporting and follow-up; champion compliant ways of working in a regulated setting.
Essential Skills/Experience:
• Degree in Mathematics (i.e., Applied Math, Engineering, etc), Statistics, Computer Science, Life Science, or equivalent experience
• Thorough knowledge of the clinical development process
• Thorough knowledge of industry standards
• Demonstrated leadership capability and proven ability to lead teams towards a common goal
• Demonstrated planning and organisational skill
• Ability to influence relevant stakeholders and global teams
• Ability to develop individuals
• Ability to manage risk in complicated or novel situations
• Current knowledge of technical and regulatory requirements relevant to the role
• Project mentality
Desirable Skills/Experience:
• Experience implementing busines
Apply on employer site ↗