Director Medical Writer
ProQR Therapeutics is a clinical-stage biotech company listed on NASDAQ with offices in Leiden, the Netherlands and Cambridge, Massachusetts, US. ProQR is focused on the development of game changing RNA therapies for severe genetic rare diseases. Our mission is to help patients by creating new medicines. A team of 160 enthusiastic ProQRians from all walks of life and more than 30 different nationalities is up to this challenge. We have the passion and commitment to make a difference in the lives of the patients we serve.
Our Regulatory Affairs department is currently looking for a Director Medical Writer (Full-time) to join our team. You will be reporting to the VP Global Regulatory Affairs.
Location: Leiden, NL
The purpose of the job of the Director Medical Writer is to oversee, prepare, write, and review scientific and regulatory documentation needed in support of research and development activities, including clinical trials and corresponding submissions to regulatory authorities and other writing and publication activities within the company. The Medical Writer contributes to strategy development for document authoring, contributes strategically and scientifically at the project and/or study team level, ensuring high-quality, scientifically accurate documents, ensures consistency between related documents, and improves overall document quality. To accomplish this, the Medical Writer liaises with different internal and external teams to execute the document development.
Key duties and responsibilities:
We expect our Director Medical Writer to have:
ProQR as an employer
We offer an exciting and innovative working environment in a very committed organization, with the following benefits:
Do you think you can contribute in achieving our mission? If so, we’re looking forward to receiving your application by filling out our application form.
Please apply as soon as possible if you are interested in this position.
You can contact Laura Faber via email@example.com if you have any questions.