Global Senior Clinical Data Management Lead

Novo Nordisk

Søborg

On-site

DKK 651,000 - 957,000

Full time

14 days+

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Job summary

Novo Nordisk in Denmark is seeking a Senior Clinical Data Management Professional to lead end-to-end data management for global clinical trials. You will own quality, integrity, and delivery from protocol to submission, collaborating across functions and portfolios worldwide.

The role demands a strong PM mindset, international trial experience, and fluent English. We offer a dynamic, patient-focused environment with opportunities to drive innovation and shape new ways of working in CDM.

Qualifications

MSc/BSc in IT, Natural or Life Sciences, or equivalent.
3+ years working within clinical data management or equivalent.
Strong Project Manager mindset and stakeholder management experience.
Good understanding of Data Management processes, clinical data flow, GCP and regulatory requirements.
Experience leading trials or projects in an international setting with increasing complexity.
Fluent in written and spoken English.

Responsibilities

Lead planning and communication trial timelines.
Align and prioritize deliverables with trial goals.
Coordinate risk and issue management with stakeholders.
Ensure project-level alignment with Project Clinical Data Manager (P-CDM).
Develop and maintain DM plans and other DM key documents.
Optimize trial design through protocol input.
Define and manage data collection requirements and risks.
Ensure data quality and integrity.
Support submission deliverables and data access processes.
Ensure regulatory and process compliance.
Ensure trial-level audit and inspection readiness and support P-CDM in project-level inspection readiness.
Support P-CDM in vendor assessments within area of expertise.