Senior Clinical Data Standards Developer (Søborg, Capital Region of Denmark, DK)

Biopharma Careers; Søborg; On-site; DKK 651,000 - 957,000; Full time

Job summary

Novo Nordisk is seeking a Senior Standards Developer to drive the end-to-end use of clinical data standards across development projects. You will contribute to governance, development, implementation, and continuous improvement of standards, enabling compliant and high-quality study execution across the organization.

You will collaborate with Clinical Data Management, Trial Management, Biostatistics, and other functions to ensure standards are captured in metadata repositories and downstream

Qualifications

• Relevant educational background in life sciences, clinical information management, pharmacy, medicine, or related field.
• 5+ years of experience in clinical data management, trial management, statistical programming, or clinical operations.
• Good understanding of GxP and the data flow from collection to submission.
• Knowledge of CRF design, Controlled Terminology, SDTM, and metadata-driven systems.
• Strong communication and collaboration across functions, cultures, and levels.
• Experience with metadata repositories or ED C systems is a plus.

Responsibilities

• Develop, maintain, and implement clinical data standards across clinical development projects.
• Support governance and operational control of standards, including CRFs and Controlled Terminology.
• Contribute to the specification and implementation of end-to-end mapped clinical data standards and related metadata.
• Interpret clinical trial designs and protocols to support accurate adoption of data standards.
• Collaborate across Clinical Data Management, Trial Management, Biostatistics, Statistical Programming, Clinical Operations, and other functions to drive standardization and compliance.
• Work with clinical metadata in relevant systems and repositories to ensure standards are captured and available downstream.

Skills

Clinical data management

GxP knowledge

SDTM

Cross-functional collaboration

Communication skills

Metadata systems

Education

Life sciences or related field

Job description

Data Standards Enablement

Søborg, Aalborg/Denmark or Bangalore/India

Are you passionate about clinical data standards?

Do you want to help shape how clinical data is collected, standardized, and used across global development programmers? Are you motivated by working at the intersection of clinical trials, metadata, regulatory requirements, and digital solutions?

Your New Role

As a Senior Standards Developer, you will play a key role in ensuring the consistent, end-to-end use of clinical data standards across Novo Nordisk clinical development projects. You will contribute to the governance, development, implementation, and continuous improvement of clinical data standards, helping to support compliant, efficient, and high-quality study execution across the organization.

In this role, you will:

• Develop, maintain, and implement clinical data standards across clinical development projects.


• Support the governance and operational control of standards, including CRFs and Controlled Terminology.


• Contribute to the specification and implementation of end-to-end mapped clinical data standards and related metadata.


• Interpret clinical trial designs and protocols to support the accurate adoption of data standards.


• Collaborate across Clinical Data Management, Trial Management, Biostatistics, Statistical Programming, Clinical Operations, and other relevant functions to drive standardization, compliance, and innovation.


• You will also work with clinical metadata in relevant systems, including metadata repositories, ensuring standards are accurately captured, maintained, and available for downstream use throughout the clinical development lifecycle.

Your New Department

Data Standards is responsible for enabling consistent, high-quality clinical data collection and standardization across clinical development. We work closely with stakeholders across the clinical trial value chain to deliver scalable standards, support efficient study execution, and contribute to robust regulatory submissions.

You will join Data Standards Enablement, a team of approximately 10 colleagues within the broader Data Standards organization of approximately 20 people. The team is characterized by strong stakeholder engagement, a collaborative mindset, and a commitment to continuous improvement and the future of clinical data standards.

Your Skills and Qualifications

To succeed in this role, we imagine that you bring a combination of clinical trial understanding, data standards knowledge, and strong collaboration skills.

We are looking for someone with:

• A relevant educational background within life sciences, clinical information management, pharmacy, nursing, medicine, veterinary science, computer science, or a comparable field.


• Preferably 5+ years of experience in clinical data management, trial management, statistical programming, clinical operations, or another relevant clinical development discipline.


• A good understanding of clinical trial conduct, GxP requirements, and the clinical data flow from data collection through analysis and submission.


• Knowledge of clinical data standards, CRF design, Controlled Terminology, SDTM, and/or metadata-driven clinical systems.


• Strong communication skills, a structured and quality-focused approach, and the ability to collaborate effectively across functions, cultures, and organizational levels.


• Experience with metadata repositories, standards libraries, EDC systems, or related clinical systems will be considered an advantage.

Working at Novo Nordisk

Every day we seek the solutions that defeat serious chronic diseases. To do this, we approach our work with determination, constant curiosity and a commitment to finding better ways forward. For over 100 years, this dedication has driven us to build a company focused on lasting change for long-term health. One where diverse thinking, shared purpose and mutual respect come together to create extraordinary results. When you join us, you're not just starting a job – you're becoming part of a story that spans generations.

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

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.

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.

What we offer

At Novo Nordisk,you'lljoin 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.

• 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: 7 September.

Please note that applications will be reviewed on an ongoing basis.

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