Medical Writer I

We are searching for the best talent for Medical Writer I to support one or more of our therapeutic areas (Oncology, Immunology, Neuroscience, and Cardiopulmonary) within the Regulatory Medical Writing unit.

As a Medical Writer I, within Regulatory Medical Writing, you will join a cohort of medical writers undertaking internal training to author a range of regulatory medical writing documents. The cohort’s target start date is 1 September 2026, and candidates must be available to commence the role at this time.

This is a hybrid position requiring three days per week on site. The role can be based in High Wycombe/ UK (moving to Maidenhead in October 2026), Beerse/ Belgium, or Leiden/ Netherlands. 

Purpose:

• Learn the regulatory medical writing role and pharmaceutical industry and business.
• Learn to work in a team environment and matrix.
• Learn internal standards, regulatory, and publishing guidelines.
• Learn internal systems, tools, and processes.
• Help to prepare sections of documents and prepare basic documents under supervision.
• Assist with routine tasks per established procedures.

You will be responsible for:

• Prepare components of clinical and regulatory documents and write basic documents such as tables of studies, narratives, protocol amendments, investigator’s brochure updates and addenda under supervision.
• May assist with document QC, abbreviations, references, literature searches, and other tasks.
• Learn how to interpret, summarize, and present statistical and medical information.
• Learn to work in a matrix environment and gain an understanding of the medical writing responsibilities on project teams.
• Attend cross-functional meetings with other writers as appropriate (eg, project kick-off and review meetings).
• Learn and adhere to SOPs, templates, best practices, policies, and Medical Writing Style Guide.
• Regularly meet with manager and mentors and attend departmental meetings.

Are you ready to join our team? Then please read further!

Qualifications / Requirements:

• A university/college degree in a scientific discipline is the minimum requirement, with an advanced degree (eg, Master’s degree, PhD, MD) preferred.
• Strong oral and written communication skills in English.
• Ability to understand and summarize scientific data.
• Ability to function in a team environment and to build solid and positive relationships with co-workers.
• Demonstrated problem-solving skills.
• Attention to detail.
• Organizational skills and time management skills.
• Demonstrated learning agility.
• Ability to learn and apply knowledge of regulatory guidance documents such as ICH requirements.
• Working knowledge of Microsoft Office programs (eg, Microsoft Word, Excel, PowerPoint, Outlook).

Required Skills:

Effective Written Communication, Graduate Education, Learning Agility, Microsoft Packages, Science Literacy

Hybrid Work