Medical Writer responsible for Clinical Disclosure

ALK-Abello; Hørsholm; On-site; DKK 500,000 - 700,000; Full time

Benefits offered by this job

Attractive working environment

Personal and professional development opportunities

Job summary

ALK-Abello in Hørsholm is looking for a driven Medical Writer to enhance clinical transparency within a collaborative team. Your role will involve preparing regulatory documents and working alongside key stakeholders to improve clinical disclosure practices.

You should have at least 3 years of experience in medical writing, an analytical mindset, and excellent communication skills. The position offers a flexible working environment, allowing collaboration on-site and opportunities for remote work.

Qualifications

• At least 3 years of medical/regulatory writing experience.
• Solid understanding of clinical development value chain.
• Experience with clinical disclosure activities.

Responsibilities

• Writing and preparing scientific and clinical documents for regulatory submissions.
• Participating in clinical trial teams and knowledge-sharing.
• Staying up-to-date with clinical disclosure legislation.

Skills

Analytical mindset

Networking skills

Collaboration

Communication skills

Medical writing

Education

Relevant university degree in natural sciences (PhD, M.Sc.)

Job description

Are you a strong networker with a drive to enhance clinical transparency at ALK? Do you thrive in a collaborative environment where your medical writing expertise can shape clinical development? Would you like to join a resilient team of medical writers in a growing company? Apply today!

The position

As part of Global Clinical Development, Clinical Reporting is a growing team of 9 enthusiastic and skilled medical writers responsible for medical writing and clinical disclosure activities across ALK.

As a Medical Writer responsible for Clinical Disclosure, you will become a central player providing clinical disclosure guidance to development projects across the product portfolio. When joining our team, part of your time will be focused on regulatory medical writing, and part of your time will be dedicated to cross‑functional work with key stakeholders to continue the development of the clinical disclosure framework and enhance the concept of transparency by design at ALK.

Your tasks will include:

• Writing and preparing complex scientific and clinical documents for submission to regulatory authorities (trial outlines, protocols, investigator brochures, clinical study reports, clinical overview and summaries, briefing packages, paediatric investigational plans, etc.).
• Participating in cross‑functional project and clinical trial teams.
• Interpreting and communicating data generated from a variety of sources, including internal and external studies and research documentation.
• Ensuring cross‑functional knowledge‑sharing related to clinical disclosure and acting as a point‑of‑contact for clinical disclosure matters.
• Staying abreast with clinical disclosure legislation and driving development and optimisation of processes, standards, and systems within Global Clinical Development.

Since physical presence enforces strong teamwork and collaboration, it is important that you enjoy coming to work at our site with a degree of flexibility to also work from home.

What you bring

To be a success in this role, you have experience working in the pharmaceutical industry coupled with an analytical mindset, well‑developed networking skills, and a drive to improve existing ways of working.

If you are attracted to the idea of implementing new initiatives across the organisation and have a passion for communicating complex data in a clear and concise manner, you may be the one we are looking for. We are driven by a high level of cross‑functional collaboration and an open‑minded approach, with a supportive team culture where everyone contributes to an inspiring and fun working environment.

We expect you to have

• A relevant university degree in the natural sciences (PhD., M.Sc., or equivalent).
• At least 3 years of medical/regulatory writing experience and a solid understanding of the clinical development value chain.
• Experience with clinical disclosure activities (registries, redaction/anonymisation, lay summaries) and a passion for staying up‑to‑date in a rapidly evolving field.
• An entrepreneurial spirit and strong collaborative skills, including a flair for training colleagues.
• The ability to thrive in a changing environment while maintaining focus on adding value and ensuring delivery on time.
• Excellent writing and communication skills (fluency in written and spoken English).

Become a part of ALK

ALK is a global pharmaceutical company specialised in allergy immunotherapy. Our offices in Denmark offer a green view of the DTU Science Park in Hørsholm.

We provide an attractive working environment for individuals looking for both personal and professional development. 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.

Apply

Apply by attaching your CV and a short letter of motivation, no later than 9 August 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 to your application documents. We evaluate applications and call for interviews on an ongoing basis, so do not wait to apply! We reserve the right to take down the advert when we have found the right candidate.

If you want to learn more about our company, we encourage you to visit us at www.alk.net. For further information regarding the position please contact Director, Clinical Reporting, Ida Mosbech Smith on [phone] (available 20-25 July and 3-7 August).

We look forward to hearing from you!