Statistical Programming Associate Director – Oncology | Full-Time | Bangalore, India
Category: Clinical Data / Biostatistics / Statistical Programming
Location: Bangalore, India
Company: AstraZeneca
Company Overview:
AstraZeneca is a global biopharmaceutical leader committed to transforming science into life-changing medicines. Our Oncology division focuses on eliminating cancer as a cause of death through innovative therapies, cutting-edge research, and evidence-based decision-making. We are dedicated to fostering a collaborative, inclusive, and high-performing work environment where talent, curiosity, and scientific rigor thrive.
Position Overview:
AstraZeneca is seeking a Statistical Programming Associate Director to lead and manage statistical programming activities within the Oncology Biometrics Programming department. Reporting to the Director of Statistical Programming, the role encompasses oversight of clinical study reports, regulatory submissions, commercialization, and scientific utilization of data to support AstraZeneca’s oncology pipeline. The position provides an opportunity to influence strategic decisions, mentor programming teams, and contribute to life-saving cancer therapies.
Key Responsibilities:
Lead and manage statistical programming activities at project and study levels.
Oversee planning, execution, and delivery of statistical programming for clinical trials.
Ensure compliance with regulatory standards and industry best practices, including CDISC standards.
Provide advanced SAS programming expertise for clinical development programs.
Collaborate with cross-functional teams, including clinical operations, biostatistics, and data management.
Mentor and guide programming teams, promoting knowledge sharing and professional development.
Contribute to strategic decision-making by leveraging clinical data insights.
Ensure quality, accuracy, and timeliness of all deliverables, including regulatory submissions and study reports.
Qualifications and Experience:
Bachelor’s or Master’s degree in Mathematics, Statistics, Computer Science, Life Sciences, or related discipline.
Minimum 10 years of experience in the pharmaceutical/biotech industry with extensive clinical trial exposure.
Advanced SAS programming skills and expertise in statistical programming for clinical trials.
Strong knowledge of CDISC standards, regulatory requirements, and industry best practices.
Proven experience in leading projects and managing cross-functional teams.
Excellent verbal and written communication skills with the ability to influence stakeholders.
Strong organizational skills and attention to detail, with the ability to manage multiple concurrent projects.
Preferred Skills:
Experience in Oncology clinical programs.
Familiarity with regulatory submissions, commercialization processes, and clinical study reporting.
Ability to drive process improvements and implement innovative solutions within statistical programming.
Why Join AstraZeneca:
At AstraZeneca, we combine courage, curiosity, and collaboration to deliver transformative oncology therapies. We offer flexible hybrid working arrangements, career development opportunities, and the chance to contribute to high-impact projects that improve patient outcomes globally.
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