JOB DESCRIPTION

Agilent Technologies is seeking an experienced Medical Writer to join our Global Clinical Affairs team in Glostrup (Copenhagen), within the Organization of Chief Medical Officer (OCMO). This role plays a critical part in supporting our medical diagnostic portfolio, ensuring compliance with the EU In Vitro Diagnostic Regulation (IVDR) 2017/746.
As a key contributor, you will be responsible for compiling and interpreting clinical performance data for all CE-marked products. Your work will support regulatory submissions and ongoing compliance efforts. You will collaborate closely with cross-functional teams including Research & Development, Quality Assurance, Regulatory Affairs, and other internal partners.

Key Responsibilities:

• Author Clinical Performance Reports for CE-marked products in compliance with IVDR (EU) 2017/746, as well as clinical research reports, abstracts, and publications
• Support the preparation and maintenance of technical documentation for regulatory submissions and audits.
• Conduct systematic literature searches to support IVDR documentation, post-market surveillance, and regulatory submissions.
• Analyze and trend External Quality Assessment (EQA) performance data.
• Research internal controlled documents and Instructions for Use (IFUs) for existing clinical performance data.
• Collaborate with internal stakeholders to compile documentation required under EU IVDR.
• Work with subject matter experts to ensure scientific accuracy and strategic alignment.
• Contribute to clinical process development and author Standard Operating Procedures (SOPs).

QUALIFICATIONS

We are looking for an experienced individual with the following background:

• Master’s degree or advanced degree in pharmaceutical, medical or relevant biomedical science fields.
• 4+ years of experience in clinical research, medical writing, or clinical science in the medical device and/or pharmaceutical industry
• Strong understanding of IVDR regulations, Good Clinical Practice (GCP) and regulatory documentation standards.
• Ability to conduct and synthesize systematic literature reviews.
• Excellent written communication skills with attention to scientific detail.
• Ability to work independently and collaboratively in a cross-functional environment.

We offer:

• Permanent Contract and Core global benefits, including the Agilent Result Bonus and Stock Purchase Plan.
• An exciting workday with many challenges, where you have the opportunity to influence processes and the way we work.
• An inspiring work environment with dedicated and competent colleagues - humor and smiles are part of everyday life!
• A good balance between work and private life.

• Author Clinical Performance Reports for CE-marked products in compliance with IVDR (EU) 2017/746, as well as clinical research reports, abstracts, and publications
• Support the preparation and maintenance of technical documentation for regulatory submissions and audits.
• Conduct systematic literature searches to support IVDR documentation, post-market surveillance, and regulatory submissions.
• Analyze and trend External Quality Assessment (EQA) performance data.
• Research internal controlled documents and Instructions for Use (IFUs) for existing clinical performance data.
• Collaborate with internal stakeholders to compile documentation required under EU IVDR.
• Work with subject matter experts to ensure scientific accuracy and strategic alignment.
• Contribute to clinical process development and author Standard Operating Procedures (SOPs)