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Tier-1 brand, mid-level 5+ years requirement, and Bangalore metro increase applicant density despite specialization.
Specialized clinical trials, SAS and CDISC requirements make skills less transferable across industries.
Explicit 5+ years requirement plus mandatory SAS, CDISC, regulatory and leadership experience.
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Provide statistical programming and lead analysis and reporting activities at the clinical study/project level within Oncology Biometrics Programming.
Develop clinical study reports, support regulatory submissions, commercialization, and scientific use of AstraZeneca product data.
Manage multiple concurrent studies/programming activities independently with accountability for technical and regulatory compliance.
Bachelor's or Master's degree in Mathematics, Statistics, Computer Science, Life or Social Sciences or related field.
At least 5 years industry experience with a Master's degree or 5+ years with a Bachelor's degree.
Extensive advanced SAS programming expertise within clinical drug development.
Good knowledge of CDISC standards and clinical trial industry procedures.
Experienced in leading studies or activities in clinical trials, demonstrating capacity to manage responsibilities at the project/study level.
Strong attention to detail with ability to handle concurrent programming tasks independently.
Effective communicator with ability to influence team members and ensure compliance with technical and regulatory requirements.