Clinical Study Manager, Clinical Operations

Lundbeck

. Lead a cross-functional global trial management team comprising colleagues from relevant Clinical Research & Development functions .

Posted 9/24/2026full-timeCopenhagen • DenmarkMid-LevelSenior💰 DKK 687,000 - DKK 944,900 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical trial management, including vendor oversight, budget management, and execution of late-phase trials across multiple geographies. Strong communication and coordination skills are essential for leading cross-functional teams and collaborating with diverse stakeholders.

Highest-signal resume keywords

Clinical Trial ManagementVendor OversightCross-Functional Team LeadershipBudget ManagementFluency in English

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Trial Project ManagementLate-Phase Trials ManagementCRO ManagementData Quality CommitmentMulticultural Collaboration

Soft Skills

Excellent Communication SkillsCoordination SkillsIndependent Work AbilityStrategic Risk ManagementCollaborative Problem-Solving

Certifications & Qualifications

MSc Degree or Higher in Medical, Pharmaceutical, or Biological Sciences

Industry Keywords

Clinical ResearchPharmaceutical IndustryPatient Advocacy GroupsGlobal Trial ManagementRare Disorder Clinical TrialsBrain Disease Clinical Trials

About the role

Key responsibilities & impact

Lead a cross-functional global trial management team comprising colleagues from relevant Clinical Research & Development functions
Collaborate with stakeholders across diverse professional, geographical, and cultural backgrounds
Work externally with clinical experts, Patient Advocacy Groups, CROs, and vendors
Serve as the primary point of contact for vendors and CROs
Ensure effective execution of clinical trials in an outsourced model
Manage vendor oversight and relationships
Deliver trial milestones in collaboration with Lundbeck colleagues
Ensure high-quality trial execution within agreed timelines and budgets
Contribute to optimizing clinical trial processes through continuous improvement
Travel approximately 20 days per year

Requirements

What you’ll need

4–8 years of trial management experience
MSc degree or higher in medical, pharmaceutical, or biological sciences (preferred candidate profile)
More than 5 years of clinical trial project management experience within the pharmaceutical industry or CRO (preferred candidate profile)
Experience managing large, late-phase trials across multiple geographies
Experience managing studies across multiple countries and sites
Experience leading global cross-functional teams
Experience managing and overseeing CROs and vendors, including budget management
Experience managing clinical trials across different developmental phases
Excellent communication and coordination skills
International experience and a multicultural mindset
Commitment to data quality and integrity
Fluency in English, verbally and in writing
Ability to work independently in a structured and proactive manner
Ability to manage deadlines and multiple priorities through strategic risk management and collaborative problem-solving
Rare disorder clinical trial experience is advantageous but not required
Brain disease clinical trial experience is advantageous but not required

Benefits

Comp & perks

Flexible working conditions
Social activities and an engaging, informal culture
Individual well-being initiatives
Exciting tasks and development opportunities
Inspiring workplace and innovative culture