Senior Clinical Data Management Professional

Clinical Data Management & Programming (CDMP)

Madrid Spain (Virtual)

Are you aclinical data managementprofessionalwith a passion forchronic diseasesDo you thrive in a global environment where yourexpertisecanturn complex clinical data into decisions that change lives

Apply now and help make data count where it matters most.

Your new role

AsaSenior Clinical Data Management Professional you will play a pivotal role inleading endtoend data management for global clinical trials with real strategic impact. You will own quality integrity and delivery from protocol to submission collaborate across functions partners and portfolios worldwide and drive innovation by challenging thestatus quoand shaping better ways of working.

Your main accountabilities will be:

• Lead planning and communicationtrial timelines.

• Align and prioritizedeliverables with trial goals.

• Coordinate risk and issue management with stakeholders.

• Ensure project-level alignment withProject Clinical Data Manager (P-CDM).

• Develop andmaintainDM plans and otherDMkey documents.

• Optimizetrial design through protocol input.

• Define and manage data collection requirements and risks.

• Ensure data quality and integrity.

• Supportsubmissiondeliverablesand data access processes.

• Ensure regulatory and process compliance.

• Ensure trial-levelaudit and inspection readiness andsupport P-CDMin project-level inspection readiness.

• Support P-CDM in vendor assessments within area of expertise

Your new department

Clinical Data Managementis responsible forthe endtoend planning execution quality and delivery of clinical trial data across Novo Nordisks global development portfolio. Operating within Clinical Data Management & Programming (CDMP) the department ensures that highquality reliable and submissionready data are generated from protocol development through database lock and regulatory submission.

The department plays a critical role inleadingtrial and projectlevel data strategies including data collection design riskbased quality management and oversight of internal and external data flows.

With a strong global footprint the department supports global trial portfolios and contributes strategically to crosstrial alignment audit and inspection readiness and submission excellence. Through close collaboration with Project Clinical Data Managers (PCDMs) and project leadershipClinical Data Management provides both operational excellence and strategic input helping transform complex clinical data into evidence that changes lives.

Your skills & qualifications

We are searching fora strategic proactive and resultsdrivenSenior Clinical Data ManagementProfessionalwithstrong integrity ethical judgment andaccountability who meet the following criteria:

• MSc/BSc in IT Natural or Life Sciences or equivalent.

• 3 yearsworking within clinical data management or equivalent.

• Strong Project Manager mindset and stakeholder management experience

• Good understanding ofData Management processesclinical data flowGCPand regulatory requirements.

• Experience leading trials or projects in an international setting with increasing complexity.

• Fluent in written and spoken English.

Moreover as a professional you are known for your analytical rigour crossfunctional collaboration operational excellence. You strive for operational excellence by challenging existing ways of working and drive the implementation of one or several innovative solutions and / or new methodologies.

Working atNovo Nordisk

At Novo Nordisk wedontwait for change. We drive dynamic company in an even more dynamic industry and we know that what got us to where we are today is not necessarily what will make us successful in the future. We embrace the spirit of experimentation striving for excellence without fixating on perfection. We never shy away from opportunities to develop weseize them. From research and development through to manufacturingmarketingand sales wereall working to move the needle on patient care.

What we offer

There is of course more on offer here than the uniqueness of our culture and the extraordinary results we produce. Being part of a global healthcare company means opportunities to learn and develop are all around us while our benefits are designed with your career and life stage in mind.

Contact

Please apply to the role via our careers site as unfortunately wedontaccept directly sent case you wish to know more about the role and the teamdonthesitate to reach outtoAndersLarsen (Associate Director Clinical Data Management Diabetes): 45-

Deadline

Apply before4May2026.

We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.

At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectivesbackgroundsand cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees the patients we serve and communities weoperatein. Togetherwerelife changing.