Global Trial Portfolio Leader
3 days ago
About Us
">At Novo Nordisk A/S, we strive to make a difference in the lives of people affected by serious diseases. We aim to transform science into life-changing medicines and we're proud to work towards this vision every day.
">Clinical Outsourcing Management
">We support Novo Nordisk's Global Trial Portfolio projects in driving and executing the clinical contracting process from request for information to signed contract, in close collaboration with internal and external stakeholders. Our team is responsible for contracting and supplier management within the clinical area and for securing a strong clinical sourcing infrastructure.
">The Role
">You will be responsible for driving the clinical outsourcing process from request for proposal to signed contract in close collaboration with our Global Trial Portfolio teams, Corporate Procurement, Legal, and external suppliers. Your tasks will include planning, initiating, and following through on Outsourcing activities for Clinical trials together with the Global trial teams, Corporate Procurement, and other stakeholders.
">Key Responsibilities
">- Plan, initiate, and follow through on Outsourcing activities for Clinical trials.">
- Collaborate with Global Trial Portfolio teams, Corporate Procurement, Legal, and external suppliers to drive the clinical outsourcing process.">
- Ensure compliance with regulatory requirements and company policies.">
About You
">You have a flair for details and an interest in improving or simplifying outsourcing processes. You are a team player and used to working in international and diverse professional groups, and you have a strong interest in business perspectives. The complexity of sourcing solutions often demands curiosity and an innovative mindset. Thinking creatively and solution-oriented is therefore a key to success.
">About the Department
">Clinical Outsourcing Management is a part of the Global Trial Portfolio in Development. Global Trial Portfolio are responsible for managing development worldwide from early clinical trials to product introduction. We ensure medical and scientific documentation for clinical submissions and authorities while ensuring that the process lives up to uniform global standards, regulations, and business ethics.
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