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The Senior Director leads global publications and scientific communications within a therapeutic area, managing a team to ensure high-quality deliverables aligned with regulatory compliance and strategic objectives.

Develop and maintain R packages for clinical trial data workflows, build Shiny applications, and promote data science best practices within the organization.

The Senior Principal Biostatistician leads statistical work for clinical trials, implements innovative designs, and provides statistical expertise for drug development.

The role involves leading translational medicine efforts for drug development in dermatology, overseeing early to late-stage clinical projects and strategies, and contributing to business development and licensing.

The role leads operational excellence in field monitoring within Novartis, focusing on strategy development, risk management, and innovation in clinical trials.

The Clinical Development Director leads strategic planning and management of clinical programs, ensuring execution of clinical development plans and overseeing deliverables while collaborating with various teams and stakeholders.

The Trial Vendor Associate Director manages vendor service delivery for clinical trials, overseeing vendor relations, budgets, and protocol reviews while ensuring compliance with GxP and ICH regulations.

The role leads regulatory strategy and submissions, oversees compliance for products, and engages with health authorities to ensure timely approvals.

Lead global regulatory strategies for development and marketed products, ensuring compliance and engaging with health authorities. Oversee submission planning and manage regulatory teams.

The GPCH leads the global clinical development program, designs strategies for regulatory approval, and manages clinical documentation. They ensure safety evaluations and collaborate with stakeholders in the realm of nephrology.