Global Clinical Study Manager: Trials & CRO Oversight

HireLifeScience; København; On-site; DKK 687,000 - 944,000; Full time

Job summary

Lundbeck is seeking a Clinical Study Specialist Manager to join our Global Trial Management team in Copenhagen. You will lead a cross-functional group within Clinical Research & Development to deliver our trial portfolio in an outsourced model.

As primary contact for vendors/CROs, you will oversee partnerships, ensure milestones are met on time and within budget, and drive continuous improvement of trial processes.

Qualifications

• MSc degree or higher in medical, pharmaceutical, or biological sciences and more than 5 years of experience in clinical trial project management within the pharmaceutical industry or CRO
• Experience in managing large, late-phase trials across multiple geographies
• Experience in managing brain disease trials is an advantage but not required
• Excellent communication and coordination skills, with international experience and a multicultural mindset
• Commitment to data quality and integrity
• Ability to communicate fluently in English, both verbally and in writing

Responsibilities

• Lead a cross-functional global trial management team comprising colleagues from relevant functions within Clinical Research & Development
• Serve as the primary point of contact for vendors/CROs, ensuring the effective execution of our clinical trials
• Responsible for vendor oversight and management, delivery of milestones in close collaboration with Lundbeck colleagues, and high-quality trial execution within agreed timelines and budgets
• As part of continuous improvement, contribute to optimizing our clinical trial processes
• Approximately 20 travel days per year should be expected

Job description

Lundbeck is seeking a Clinical Study Specialist Manager to join our Global Trial Management team in Copenhagen. You will lead a cross-functional group within Clinical Research & Development to deliver our trial portfolio in an outsourced model.

As primary contact for vendors/CROs, you will oversee partnerships, ensure milestones are met on time and within budget, and drive continuous improvement of trial processes.