Hobson Prior are currently looking for a Senior Medical Writer to join an exciting company on a permanent basis. Our clients focus on providing services that are within the field of regulatory affairs.

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

Key Responsibilities:

• Writing high-quality regulatory documents. Such as IB, CTD summary documents and overviews.
• Orphan Drug applications, RMPs, and PIPs.
• Accumulate any documentation required for approval and conduct of clinical studies. Documentation to support agency meetings (briefing books, presentations).

Requirements:

• The ideal candidate will require an advanced degree in life sciences, medicine or veterinary medicine.
• A minimum of 5 years' experience in medical writing on wide range of regulatory documents.
• You will require an understanding of FDA and ICH regulations and guidelines.
• The candidate will have the ability to work independent, analyse and summarise data (clinical, non-clinical, quality).
• Ability to manage multiple tasks simultaneously under time constraints.
• Excellent communication skills in English and a second language, preferably German.
• Strong knowledge of 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.