Senior Clinical Data Management Professional

CDMP Clin Pharm

Søborg, Denmark

Do you thrive in a dynamic and collaborative environment where you can combine operational excellence, stakeholder management, and scientific insight? If so, this could be an exciting opportunity to join Clinical Data Management in Clinical Data Management & Programming ClinPharm at Novo Nordisk.

We are looking for a Senior Clinical Data Manager to join our team on an 18-months temporary assignment and contribute to the execution of complex clinical pharmacology trials that support the development of new treatments for people living with serious chronic diseases.

The Position

As Senior Clinical Data Manager, you will be accountable for planning, coordinating, and delivering data management activities across one or more clinical trials within Clinical Pharmacology. You will play a key role in ensuring data quality, integrity, and timely delivery of clinical trial data throughout the study lifecycle.

Working closely with cross-functional colleagues, vendors, and global stakeholders, you will act as the Data Management lead for assigned trials and serve as a key point of contact for data-related decision making.

Your key responsibilities will include:

• Leading Data Management activities from study start-up through database lock and submission readiness.
• Driving planning, execution, and delivery of Data Management trial deliverables.
• Defining and overseeing data collection strategies, standards, and quality plans.
• Managing risks, issues, and dependencies related to trial data.
• Collaborating with Clinical Pharmacology colleagues, statisticians, programmers, study teams, and external partners.
• Ensuring compliance with ICH-GCP, regulatory requirements, and Novo Nordisk processes.
• Contributing to continuous improvement initiatives and the implementation of innovative ways of working.
• Supporting inspection and audit readiness activities.

In this role, you will have the opportunity to influence both trial execution and future Data Management practices through your expertise and proactive approach.

Qualifications

To succeed in this role, you should have:

• A degree (BSc, MSc, or equivalent) in Life Sciences, Health Sciences, Data Science, Information Technology, or a related field.
• More than three years of experience within Clinical Data Management in the pharmaceutical, biotechnology, or CRO industry.
• Solid understanding of clinical trial processes, clinical data flow, and regulatory requirements including ICH-GCP.
• Experience leading Data Management activities for complex clinical trials.
• Strong project coordination and stakeholder management skills.
• Experience working in cross-functional and international environments.
• Fluency in written and spoken English.

As a person, you are:

• Self-driven and proactive with an innovative mindset.
• Structured and able to manage multiple priorities simultaneously.
• Analytical with a strong focus on quality and continuous improvement.
• Collaborative and effective at building relationships across functions.
• Comfortable navigating complexity while keeping solutions simple and pragmatic.
• Experience from clinical pharmacology studies, early-phase development, or innovative trial designs will be considered an advantage.

About the Department

You will join the Clinical Data Management team within Clinical Pharmacology, a global organization responsible for delivering high-quality clinical data that enable informed decision making throughout drug development.

The department consists of highly skilled Clinical Data Managers as well as Clinical Data Scientists who work closely with scientists, clinicians, statisticians, programmers, and external partners across the globe. Together, we are committed to ensuring data quality, operational excellence, and continuous innovation in how we support clinical development.

We offer a collaborative and inclusive environment where knowledge sharing, professional growth, and teamwork are central to how we work.

Working at Novo Nordisk

At Novo Nordisk, we don't wait for change. We drive it. For more than 100 years, we have been translating unmet medical needs into innovative medicines and delivery systems that improve the lives of millions of people worldwide.

Working here means joining a company committed to changing lives while investing in your development and creating opportunities for you to grow professionally and personally.

What we offer

At Novo Nordisk, you'll join a global healthcare company with a unique culture and strong results. We offer continuous learning, career development, and benefits tailored to your life and career stage.   

Salary:  For this role, the Annual Base Salary ranges from 651,000.00 to 956,900.00 DKK, corresponding to the level of the position.

The placement within the salary range will be assessed during the recruitment process based on the candidate’s skills, competencies, knowledge, and relevant experience.

Incentives and Benefits: The salary package may include short-term and/or long-term incentives as well as other employee benefits based on position level, location, functional area and relevant market benchmarks.

Learn more about our Reward Philosophy here

Deadline

16th August

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

At Novo Nordisk, we're not chasing quick fixes – we're creating lasting change for long-term health. For over 100 years, we've been driven by a single purpose: to defeat serious chronic diseases and help millions of people live healthier lives. This dedication fuels our constant curiosity and inspires us to push the boundaries of what's possible in healthcare. We embrace diverse perspectives, seek out bold ideas, and build partnerships rooted in shared purpose. Together, we're making healthcare more accessible, treating and preventing diseases, and pioneering solutions that create change spanning generations. When you join us, you become part of something bigger – a legacy of impact that reaches far beyond today.