Summary
You will oversee and coordinate early modeling viability assessments, global feasibility assessments, recruitment projections, and allocation strategies for assigned trials and programs
About the Role
#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.
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Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.
