Expert Regulatory Writer
ProClinical is working with a top 5 pharmaceutical company based in Basel with an enviable commercial portfolio, rich tradition of drug development and world leading pipeline.
The position here will be based in their global HQ in Basel and will be in a specialist regulatory writing team working across multiple therapy areas. You will be responsible for authoring high quality clinical summaries and overviews for MII (Module II) and authoring of clinical study reports (Module V).
Skills and Requirements:
- You must have experience of authoring such sections of the dossier in preparation for major submissions of NCE/NBE.
- In addition, you should have worked in a matrix environment and understand the general drug development process in detail.
- On offer is an exceptional opportunity to join a world leading company in a highly skilled team with excellent career growth opportunities available in the long term.
Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.
In case you have difficulty in applying or if you have any questions, please call David Nixon on +44 203 078 9544 or upload your CV on our website - www.proclinical.com.
A full job description is available on request.
ProClinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.