Lead global medical affairs study operations, overseeing study management teams, budget planning, and fostering a culture of empowerment and collaboration.

As a Brand Manager for Immunology, you will drive brand strategy, oversee product launches, manage budgets, and collaborate with teams to maximize market performance.

The Director of Pipeline Intelligence and Reporting drives data analysis and reporting to influence strategic decisions in drug development, ensuring efficient pipeline management and collaboration across teams.

The Senior Risk Surveillance Lead drives Risk-based Quality Management in clinical trials, overseeing risk surveillance, quality governance, and continuous improvement across trial protocols and teams.

The Clinical Quality Assurance Program Lead provides oversight for clinical trials ensuring compliance with regulations, quality strategy implementation, and risk management while leading QA initiatives and collaborating with global teams.

Lead medical safety strategies and teams for clinical development projects, ensuring compliance and safety management throughout drug development.

Oversee authoring, formatting, and publishing of Clinical Study Report (CSR) appendices, ensuring compliance with regulatory standards and improving submission processes. Manage vendor oversight and collaborate with cross-functional teams to enhance document readiness and quality.

The Vendor Performance Analysis Manager analyzes business processes to optimize costs, improve supplier performance, and supports sourcing strategies. Responsibilities include data analysis, financial modeling, and collaboration with cross-functional teams to enhance operational efficiency and vendor relationships.

The Associate Director will lead genetic toxicology studies, provide expert assessments, ensure regulatory compliance, and collaborate with teams on drug development.

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 Global Program Associate Director manages global drug development programs, oversees project strategy, identifies risks, coordinates documentation, and ensures effective team communication.

Accountable for GCP compliance oversight in Global Clinical Operations, managing audits, inspections, quality issue resolution, and promoting compliance culture.

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.