Global Clinical Study Lead (Specialist) - Trials & Vendors

Lundbeck; København; On-site; DKK 687,000 - 945,000; Full time

Job summary

Lundbeck is seeking a Clinical Study (Specialist) Manager based in Copenhagen to lead a global trial management team and oversee CROs and vendors. This role drives study delivery across multiple countries with a focus on timelines and budgets.

You will work in Clinical Operations, coordinating across diverse stakeholders and ensuring data integrity. The role requires strong leadership, warm collaboration, and fluency in English in an inclusive, cross-cultural environment.

Qualifications

• MSc degree or higher in medical, pharmaceutical, or biological sciences.
• More than 5 years of clinical trial project management experience.
• Experience managing large late-phase trials across multiple geographies.
• Experience in managing brain disease trials is an advantage but not required.
• Excellent communication and coordination in an international context.

Responsibilities

• Lead a cross-functional global trial management team.
• Oversee CROs and vendors, including budget oversight.
• Manage multi-country studies and timelines in development phases.
• Collaborate with diverse stakeholders to ensure quality, compliance and delivery.
• Communicate effectively with internal teams and external partners.

Skills

Trial management

Vendor oversight

Budget management

Cross-functional teams

Education

MSc or higher in medical/pharmaceutical/biological sciences

Job description

Lundbeck is seeking a Clinical Study (Specialist) Manager based in Copenhagen to lead a global trial management team and oversee CROs and vendors. This role drives study delivery across multiple countries with a focus on timelines and budgets.

You will work in Clinical Operations, coordinating across diverse stakeholders and ensuring data integrity. The role requires strong leadership, warm collaboration, and fluency in English in an inclusive, cross-cultural environment.