Clinical Operations Strategist

4 days ago


Copenhagen, Copenhagen, Denmark Novo Nordisk AS Full time

About Us


Clinical Operations at Novo Nordisk A/S is responsible for setting up and executing phase 1-4 clinical trials within our area. We are a global network with collaboration, knowledge sharing, talented colleagues, and challenging assignments in a dynamic project-centric organization. Our environment offers continuous personal and professional development opportunities.



Job Description

We are seeking an experienced Senior Clinical Operations Manager to lead from a strategic point of view the execution of clinical projects in assigned therapeutic areas in all countries of Region Europe & Canada (EUCAN). Your responsibilities will include following up on trial status, motivating, supervising, and supporting team members. You will also coordinate communication related to projects with Clinical Development & Project Leadership (CDPL), International Operations Strategic Office (IOSO) Clinical, and internally in the region.



Main Accountabilities:

  • Lead Strategic Planning: Develop/update strategic plans with countries in the region, involving stakeholders and ensuring implementation.
  • Trial Portfolio Review: Lead process of Trial Portfolio Review (TPR) in the region and coordinate feedback with Centre Development Centres (CDCs) or countries to Global Trial Planning.
  • Country Allocation: Provide input and ensure alignment in country allocation process, in close contact with Global Trial planning, CDPL project teams, CDCs, and countries.
  • Recruitment Follow-up: Responsible for follow-up recruitment versus plans and coordinating re-allocations in and out of the region.
  • Medical Support: Coordinate with regional medical managers and CDC Clinical Medical Managers to ensure adequate medical support to projects.
  • Improvement/Strategic Projects: Lead improvement/strategic projects across the region.


Requirements

To be successful in this role, you should have:



  • Bachelor's Degree, Master's degree, or PhD in Life Sciences.
  • Advanced Clinical Research Associate and project management level, trained in Good Clinical Practice.
  • Minimum 5 years of working experience in clinical project management.
  • Solid knowledge of clinical development processes.
  • Fluent in written and spoken English.
  • Team-oriented personality with high degree of flexibility, proactivity, independence, and cross-cultural awareness, as well as good presentation and communication skills.
  • Solid knowledge of Excel and other tools to track metrics.


The scope of this position is all countries within Region EUCAN executing Product Development Plan trials.



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