Global trial manager

BH-332107
  • Competitive
  • Denmark Copenhagen
  • Contract
  • Life Sciences
Our client in Denmark is currently looking for a Global Trial Manager with the description below.
Duration: 12 Months with extension possible

About the job
Do you want to be part of a high-performing global development team and help bring new treatments to patients with diseases? This is a chance to work on innovative therapies, including treatments for rare conditions where there are currently limited or no options.

We are looking for a Global Trial Manager to join the team.

Your Role
As a Global Trial Manager, you will be part of the global Clinical Operations team and play a key role in the delivery of international clinical trials.
You will lead a cross-functional trial team and work closely with internal colleagues across Clinical Research & Development. You will also collaborate with external partners such as clinical experts, Patient Advocacy Groups, CROs, and other vendors.
In this role, you will be the main point of contact for CROs and vendors, ensuring clinical trials are delivered effectively and to a high standard. You will oversee external partners, manage their deliverables together with internal stakeholders, and make sure trials are executed on time, within budget, and with strong quality.
You will also contribute to improving clinical trial processes and ways of working.

Your responsibilities
  • Lead global trial management activities across clinical studies
  • Manage and oversee CROs and vendors, including budgets and deliverables which is crucial
  • Coordinate cross-functional teams and keep stakeholders aligned
  • Support trial delivery across different study phases
  • Manage studies across multiple countries and sites
  • Work closely with external partners such as service providers, advisors, and vendors
  • Drive trial progress in a structured and proactive way
  • Handle timelines, priorities, risks and challenges through clear communication and problem-solving
Your profile
  • MSc degree or higher in medical, pharmaceutical, biological or a related life science field
  • Around 10 years of experience in clinical trial project management within a pharmaceutical company or CRO
  • Strong experience managing large late-phase clinical trials across multiple regions including both the EU and US
  • Experience with rare disease trials is an advantage
  • Strong communication and coordination skills with experience working in international and multicultural environments
  • High attention to data quality and integrity
  • Proactive, structured, and goal-oriented with strong stakeholder management skills
  • Fluent in English, both written and spoken


With over 90 years' combined experience, NES Fircroft (NES) is proud to be the world's leading engineering staffing provider spanning the Oil & Gas, Power & Renewables, Chemicals, Construction & Infrastructure, Life Sciences, Mining and Manufacturing sectors worldwide. With more than 80 offices in 45 countries, we are able to provide our clients with the engineering and technical expertise they need, wherever and whenever it is needed. We offer contractors far more than a traditional recruitment service, supporting with everything from securing visas and work permits, to providing market-leading benefits packages and accommodation, ensuring they are safely and compliantly able to support our clients.

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