In this leadership role, you will drive strategic planning and operational excellence, manage portfolios, oversee strategic projects, and serve as a trusted advisor to senior leadership, ensuring successful product launches and alignment with organizational goals.

Lead and co-manage cross-functional clinical trial teams to plan, execute, and deliver medium-to-complex global clinical studies. Oversee operational strategy, timelines, budgets, risk management, vendor and local-team relationships, inspection readiness, and study close-out while promoting process improvement and an agile culture.

The Chief Scientific Officer leads medical strategy for Novartis, managing medical affairs teams, ensuring compliance, and building partnerships to enhance healthcare outcomes.

The Clinical Development Director leads clinical programs, ensuring delivery of clinical goals, collaborating across teams, managing trial data, and contributing to regulatory documents amidst a focus on patient safety.

As a REP Lead, you will lead a recruitment team, drive hiring strategies, ensure process excellence, and improve candidate experience and team performance.

The role involves leading clinical data management tasks, ensuring quality and compliance in data for clinical trials, collaborating with teams, and supporting junior staff.

Lead the design and delivery of AI-driven projects in Marketing, collaborating with stakeholders to innovate and manage prototypes and MVPs.

The Central Monitor oversees clinical trials via data surveillance and centralized monitoring, ensuring data quality and regulatory compliance.

The Lead Central Monitor oversees clinical trial monitoring by managing a team, developing strategies, ensuring data integrity, and fostering collaboration. They drive risk management and process improvements while supporting clinical trial teams in their execution.

The Game Studio Solutionist will design and develop interactive experiences, rapidly prototyping digital solutions while collaborating across teams and ensuring quality and compliance.

The role supports communication and governance by managing content calendars, creating content, facilitating approvals, and collaborating across teams to improve processes.

Manage planning, coordination, and execution of scientific engagement activities (advisory boards, congresses, EEEs, medical education). Translate strategy into operational plans, manage logistics and vendors, ensure compliance and audit-ready documentation, identify process improvements, and coordinate cross-functional stakeholders to deliver high-quality scientific engagements.

The Senior Scientific Writer II develops and delivers scientific materials, collaborates with cross-functional teams, and ensures compliance with quality standards in therapeutic areas such as Oncology, Cardiovascular, Renal, Neuroscience, or Immunology.

The Global Program Clinical Head leads clinical programs in neuroscience, overseeing strategies and execution for regulatory approvals and market access, interacts with stakeholders, and ensures team development.

Lead end-to-end development of high-quality scientific materials (slide decks, congress content, advisory board resources), synthesize complex clinical data into clear messaging, ensure scientific accuracy and governance compliance, and collaborate across global matrix teams to harmonize content and support lifecycle management.

As an Expert Scientific Writer, you will create high-quality scientific content, manage projects from brief to publication, and mentor team members while ensuring compliance and quality standards.

The Head of Scientific Learning & Capability leads the design and implementation of capabilities across International Medical Affairs, enhancing performance through learning strategies and programs while collaborating with cross-functional teams and managing external partnerships.

The Principal Clinical Data Scientist manages Data Management for clinical studies, ensuring compliance with good practices, leading quality deliverables, and implementing training strategies.

The Global Program Associate Director will manage global drug development projects, facilitating strategies, communication, and issue resolution while ensuring effective operation of the Global Program Teams.

The Senior Scientific Engagement & Program Manager plans and executes medical engagement activities, ensuring quality delivery across therapeutic areas by managing projects and collaborating with cross-functional teams.