Senior Medical Writer - Regulatory - Switzerland
- Contract Type
Our client is a Bio Pharma who are full of colour and creative edge, their R&D pipeline is full, and they have a bright future ahead of them. To be part of this very exciting journey please contact firstname.lastname@example.org or call me for a confidential conversation on +44 207 255660
This is an exciting opportunity to join an innovative Bio pharma in Switzerland who are creative and bursting with ideas.
Your own creativity, imagination and passion for all things scientific will be right at home here. You will be responsible for writing and overseeing the writing of complex regulatory documents for submission to regulatory authorities in support of drug development and marketing applications. Contribute scientifically and strategically at the project and/or study team level to facilitate efficient development of high-quality clinical documents for regulatory filing as well as be further responsible for training and mentoring more junior individuals within the team.
To be considered for this role you will need to have at 5 years’ experience in all aspects of regulatory writing, ideally during all phases of drug development and commercialization (investigational, registration, pre- and post-launch, marketed). This can be from Pharma or Agency. Fluent English is needed both spoken and written.
If successful in securing the role of Snr Medical Writer you will be offered a low hierarchical, team-oriented work atmosphere with scope for independence; exposure to an interesting and broad range of activities and a competitive and attractive remuneration package.
Knowledge is power
To find out more about this excellent opportunity apply today. If you would like a confidential conversation on how this role will fit with your own needs or experience, then please do get in touch. I can be reached on email@example.com or on +44 207 255 6600.