#LI-Hybrid

Location: London UK and Dublin Ireland

The Global Feasibility Lead / Clinical Operations Program Manager is responsible for provide operational support for clinical development programs and trials where there are early viability, feasibility, allocation and site selection activities to deliver. This role supports Clinical Operations Program Director or Associate Director (COP(a)D) for the assigned feasibility assessments and allocation strategies of trial(s).

This role is based in London UK or Dublin Ireland. Novartis is unable to offer relocation support for this role: please only apply if this location is accessible for you.

Key requirements

• Analyze various data sources, including clinical trial data, historical performance, publications, epidemiology, clinical trial and commercial landscape, etc.

• Provide modeling and viability analysis to support early recruitment projections and clinical trial planning

• Conduct end to end clinical trial feasibility in collaboration with the country feasibility managers, clinical trial team and medical teams

• Propose optimal country and site allocation, including associated risks and opportunities in alignment with the global program strategy

• Provide feedback on study design based on available data and feasibility insights

Essential requirements

• Degree in Life Sciences or related scientific discipline

• 2-3 years pharmaceutical clinical drug development experience

• Solid understanding of all aspects of clinical drug development with particular emphasis on clinical trial design and trial execution

• Demonstrated experience in data driven feasibility for global clinical trials

Desirable Requirements

• Has had success in identifying, proactively flagging, and resolving risks; experience with strategic scenario planning and management.

• Communicates effectively with colleagues in a local/regional/global matrixed environment.

• Good project management capabilities with demonstrated ability to problem solve and mediate issues.

• Ability to understand analytical data insights with proven ability to communicate background details and rationale.

• Basic knowledge of the international aspects of drug development process, the international standards (GCP/ICH), health authority regulations, and clinical development process.

• Strong skills in MS Office Suite including: MS Teams, Excel, Word

Commitment to Diversity and Inclusion / EEO paragraph

Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.