Manager - Statistical Programming

Design, develop, and implement technical solutions for integrating, analyzing, and reporting clinical data to support regulatory approval and market acceptance of products.

Provide comprehensive programming support including development of programming strategies, standards, specifications, and analyses for clinical projects.

Collaborate with cross-functional teams, external vendors, and leadership to ensure quality, compliance, and alignment with clinical development objectives.

5 - 8 years clinical/statistical programming experience within pharmaceutical clinical development.

Undergraduate or Graduate degree in statistics, biostatistics, mathematics, computer science or equivalent experience preferred.

Significant knowledge of SAS software (Base, Stat, Graph) and clinical drug development processes.

Oncology experience preferred (not strictly mandatory).

Experienced in clinical trial programming with a strong understanding of drug development, clinical trial methodology, and global regulatory requirements.

Ability to lead programming strategy and maintain compliance with regulatory standards in cross-functional and vendor interactions.

Proven ability to organize multiple assignments, adapt to changing priorities, and communicate effectively within global teams.