Senior Manager, Medical Writing, Clinical to Launch

Senior Manager for Regulatory Writing, Clinical to Launch, Cash Rich Pharmaceutical Company Expanding Operations in Europe

We have been given a mandate to recruit for an experienced regulatory writer who can lead a group of technical writers for upcoming and critical regulatory submissions. The company are still relatively small in Europe and as such have a small pharma environment in their Zug office. For those who are tired of big pharma or consultancies, it could be an excellent move to gain real autonomy and be in a company where your impact will be clearly seen! Please contact me should you be interested.

Essential Duties and Responsibilities:

• Author, review, and/or edit departmental documents (e.g., protocols, reports, regulatory filings, scientific publications/posters) for scientific accuracy and clarity;
• Ensure pharmaceutical development documents and templates comply with company and regulatory standards for style and format;
• Manage the pharmaceutical development documentation review process;
• Supervise technical writing personnel in the writing group

Job Requirements:

Education: MS/PhD or equivalent proven track record/competence

Experience: 8 or more years of relevant industry experience. Scientific background and previous medical, technical or scientific writing and research necessary. Experience with regulatory filings (IND, NDA, MAA) is needed.

For a confidential discussion about this role, or to apply, then send your CV to m.beedle@nonstop-recruitment.com or call me, Matt Beedle, on +41435 080817.

NonStop is one of the largest and fastest growing specialised life sciences recruitment companies in Europe. We are proud members of the APSCo life sciences group who ensure we meet the highest quality standards within the recruitment industry. Our offices are located in the UK, Switzerland and the Czech Republic and we hold labour leasing licences across Europe. Please visit our website for a full list of the niche markets we cover.