Senior Clinical Data Lead - Global Trials & Quality

Novo Nordisk A/S; Aalborg; Hybrid; DKK 651,000 - 957,000; Full time

Job summary

Novo Nordisk A/S in Denmark seeks a Senior Clinical Data Management Professional to lead end-to-end data management for global clinical trials, from protocol development to submission. You will combine hands-on trial leadership with strategic thinking, uniting functions and partners to manage complexity, strengthen data quality and develop better ways of working.

You will own data management activities across the trial lifecycle, shaping protocols, data collection requirements and risk

Qualifications

• A BSc or MSc in IT, Natural Sciences, Life Sciences or an equivalent field.
• At least 3 years of experience within clinical data management or an equivalent area.
• Experience leading trials or projects in an international environment with increasing complexity.
• Strong project management and stakeholder management skills.
• A good understanding of data management processes, clinical data flow, Good Clinical Practice (GCP) and regulatory requirements.
• Fluency in written and spoken English.

Responsibilities

• Lead data management planning, timelines and priorities, aligning deliverables with overall trial goals.
• Develop and maintain data management plans and other key trial documentation.
• Shape effective trial design by providing data management input to protocols and defining data collection requirements and risks.
• Drive data quality and integrity while coordinating risks and issues with relevant stakeholders.
• Support submission deliverables, data access processes, regulatory compliance, and trial-level audit and inspection readiness.
• Partner with the Project Clinical Data Manager on project-level alignment, inspection readiness and vendor assessments within your area of expertise.

Skills

Project management

Stakeholder management

Data management

GCP

English proficiency

Education

BSc/MSc in IT or Life Sciences

Job description

Novo Nordisk A/S in Denmark seeks a Senior Clinical Data Management Professional to lead end-to-end data management for global clinical trials, from protocol development to submission. You will combine hands-on trial leadership with strategic thinking, uniting functions and partners to manage complexity, strengthen data quality and develop better ways of working.

You will own data management activities across the trial lifecycle, shaping protocols, data collection requirements and risk