Great opportunity to move to Switzerland and enjoy all the benefits living in a safe environment whilst enjoying the higher quality of life and all other advantages this country has to offer in the future.
You will also have a variety within your role working autonomously and developing your experience even further.
Your main responsibilities will include writing documents owned by regulatory in collaboration with other functions (e.g. the IMPDs, INDs, Briefing Books, ODDs, PIPs or similar for the US, FTDs, BTDs and IND annual reports) as well as contributing to reviewing/editing documents owned by other functions (e.g. clinical protocols, IBs, DSURs, CSRs…).
I would love to discuss this opportunity further if you have relevant experience:
• Bachelor’s degree in a scientific discipline; post-graduate scientific degree is preferred
• Minimum 5 years experience in medical writing with through understanding of regulatory requirements, drug development and medical writing processes
• Good experience in writing regulatory documents such as briefing books, IMPDs, INDs
Please bear in mind that this role is located in Switzerland so a local candidates as well as candidates from UK and EU member states are welcome.
Please forward your CV in the Word format to Oksana Kolesnichenko or recommend this role to someone who would be suitable at (url removed).
If you do not hear from me you might not have the exact skills required for the position, however, I will make sure to keep your profile for any other possible opportunities.
The job market changes very quickly so do not forget to connect with me on Linked in, check out other roles that I am hiring for at the moment and follow for any future relevant openings.
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