Clinical Data Manager

Would you like to have a key role in clinical development at ALK and help shape how we collect and process the data of our clinical trialsDoes it appeal to you to contribute to the data deliverables that are at the core of ALKs current and future products across programs in North America Europe and China.

The position
As a Clinical Data Manager you will join our Clinical Data Management group which builds and maintains clinical databases electronic Case Report Forms (eCRFs) and Data Management Plans that ensure every trial produces high-quality reliable data. The group is part of Biometrics within a broader Clinical Data Science function in Global Clinical Development.

This is a hands-on role. You will be directly involved in keeping trials running - monitoring incoming data resolving queries managing discrepancies and making sure the data is clean complete and delivered on time.

We are also investing in how clinical data management works - including data governance platform development and structured approaches to automation. Were looking for someone who is genuinely curious to explore this evolving area and eager to grow with us in this direction while also engaging in core hands-on responsibilities.

Your primary tasks will be:

• Study data oversight. You will be responsible for accurate timely and complete data collection entry and validation for assigned studies. You are the person who knows the state of the data and can explain it to the project team.
• Database management. Development testing live maintenance and compliance with ALK SOPs and regulatory requirements. You will work with the EDC systems where our trial data lives - building configuring and maintaining clinical databases.
• Data quality control. Implement and run data checks. Manage discrepancies. Resolve data queries with clinical sites and monitors. Ensure data integrity throughout the study lifecycle. This is detailed hands-on work and it matters - data quality issues caught late cost time and trust.
• Collaboration. Work closely with biostatisticians statistical programmers clinical operations and external vendors on study setup data transfers ongoing documentation and training support. You are a connector between the data and the people who use it.
• Documentation and compliance. Maintain Data Management Plans validation documents edit check specifications and all audit-required records
• Reporting. Generate data listings status summaries and support interim and final analysis with clean well-structured deliverables.
• Support project timelines. Identify escalate and help mitigate risks to ensure on-time and high-quality deliverables across your assigned studies.
• Contribute to how we work. Support internal projects in data standards (eCRF eDiary lab data) data governance and our evolving systems and platforms. As you learn the current processes we want you to ask whether they could work better - and be willing to help find out.

Your profile
You have a STEM background at BSc level or higher in a relevant discipline - natural sciences health sciences data science IT or similar. Moreover bring:

• Hands-on and detail oriented. You are comfortable working with data at a granular level - cleaning checking querying resolving. You take ownership of the quality of what you deliver.
• Some experience in clinical data or a strong willingness to learn. Two to three years in clinical development (pharma or CRO) is ideal. If you come from a different data-intensive background that works too.
• Familiarity with programming and data tools. Working knowledge of Python R or SAS. You do not need to be a developer but you need to be comfortable working with code writing queries and handling structured data. The direction of this field is increasingly technical and this role will grow with it.
• Organized and reliable. You can handle multiple studies and competing priorities keep track of timelines and flag risks early. The team can depend on you to deliver.
• Good communication skills. Fluent in written and spoken English. You will interact with clinical sites monitors statisticians and vendors.
• Curious. You want to understand how the systems you work with function. You notice when a process could be improved. You are open to new tools and new approaches.

Become a part of ALK
We provide an attractive working environment for individuals looking for both personal and professional development. ALK is a global pharmaceutical company specialised in allergy immunotherapy. We are driven by a high level of professionalism integrity an openminded approach and contributing to an inspiring and fun working environment together with our colleagues. You will be part of an engaged and informal team who values skill and knowledge creation. The result of your efforts will be significant throughout the organisation and you will be able to actively influence and challenge the status quo.

Our offices in Denmark offer a green view of the DTU Science Park in Hørsholm. We believe that physical presence enforces strong teamwork and collaboration and creates success so it is important that you enjoy coming to work at our site with a degree of flexibility to also work from home.

Do you want to learn more about our company we encourage you to visit us at .

Apply
Apply by attaching your CV and a short letter of motivation no later than 3 May 2026.

We commit to an inclusive recruitment process and equal opportunity for all our job applicants. Hence we prefer that you do not add images in your application documents. We evaluate applications and call for interviews on an ongoing basis so dont wait to apply! We reserve the right to take down the advert when we have found the right candidate.

We are looking forward to hearing from you!