Hobson Prior are looking for a Senior / Medical Writer to join a brilliant CRO on a permanent basis located in Munch with the flexibility to work on a hybrid basis. Our client is focused on providing a varied assortment of services in the areas of regulatory affairs.

Please note that to be considered for this role you must have the right to work in this location.

Key Responsibilities:

• As the Senior / Medical Writer, you will be responsible for Orphan Drug submissions, RMPs, and PIPs.
• Assemble any reports needed for consent and perform clinical studies.
• To assist with agency meetings, you will handle reports such as briefing books and presentations.
• Accountable for writing high-quality supervisory papers, for example: IB, CTD summary reports (2.6, 2.7) and outlines (2.4, 2.5).

Key Skills:

• Work well independently with the ability to assess and summarise data such as clinical, non-clinical and quality.
• Capable of handling multiple tasks concurrently with the ability to meet deadlines.

Requirements:

• Educated to an advanced degree level in a life science, medicine or veterinary medicine discipline.
• At least 5+ years of experience in medical writing a broad variety of regulatory papers.
• Comprehension of FDA and ICH protocols and procedures.
• Communication skills with fluency in the English and German language, though any second language is acceptable.
• Computer literacy in Microsoft Office and graphical software.

Apply now:

If you are interested in learning more or applying to this exciting opportunity then please click "Apply" and upload a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist directly, please select "Contact me" at the top of this page.

Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.