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Lead Phase III oncology and hematology trials, manage teams, drive project success, mentor staff, and ensure quality and regulatory compliance.

Coordinate and manage clinical research projects, ensuring compliance with regulations, recruiting participants, maintaining documentation, and supporting the principal investigator. Handle logistics, monitor study progress, and facilitate communication within the team.

The role involves developing and maintaining R-based applications, mentoring biostatisticians, overseeing projects, and ensuring statistical quality and compliance in clinical trials.

The Veeva RIM Administrator - Manager will oversee regulatory systems, document requirements, support validation teams, and educate users on system processes.

Perform data entry, tracking, verification, and quality control checks for a clinical trial database while maintaining confidentiality. Assist with system improvements and training material preparation.

The Principal Biostatistician leads biomarker analysis for clinical studies, develops evaluation plans, conducts data analyses, mentors staff, and ensures accurate statistical deliverables while collaborating across teams.

The Internal Account Director develops and implements recruitment and retention strategies, collaborates with teams to meet customer goals, and analyzes market trends for product improvements.