|Job title :||Senior Regulatory Writer - partial home based - London UK|
|Job type :||Permanent|
|Salary :||Highly competitive market related|
|Contact name :||Harriet Lawford|
|Contact email :||email@example.com|
This is an exciting opportunity for a Senior Medical Writer (can consider Principle Medical Writer) - Regulatory to join a Global Biotech Company in central London, UK 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 least 3 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/ CRO 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 (inclusive of company shares).
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 firstname.lastname@example.org or on .