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The Clinical Trial Manager II oversees site management and clinical monitoring activities, ensuring compliance with protocols and regulations, and coordinating with various functional leaders to meet study milestones.

Lead statistical programming efforts, managing a team, developing programming code in SAS, ensuring data integrity, and mentoring junior programmers.

The role involves managing regulatory submissions and activities, including gap analyses, product development plans, and agency interactions, while providing support and training internally and externally.

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

The Site Contracts Specialist II manages contract processes for clinical trials, negotiates contracts and budgets, and collaborates with cross-functional teams. Responsibilities also include training staff and ensuring compliance with regulations.

The Sr. Project Specialist oversees project files, maintains study data, coordinates meetings, tracks KPIs, ensures document archiving, and supports audits while mentoring Project Specialists. Bilingual proficiency in French and English is required.

Assist in document publishing and quality control tasks in regulatory publishing. Collaborates with teams to create and submit compliant documentation to regulatory authorities.

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 Sr Director of Operations oversees client relationships and project teams, ensuring operational excellence and strategic alignment in Real World Late Phase studies.

The Sr. Clinical Trial Manager oversees clinical trial management processes, ensuring compliance, managing risks, and coordinating teams to achieve project milestones in clinical research.