Client: An expanding biotech with a strong presence across the U.S and Europe
Location: East coast USA
Package: Salary varies up to $200,000 basic for experienced candidates (levels may differ based on experience)
We have worked closely for many years with this client filling various cross-functional/vertical positions and have now opened up clinical and regulatory/writing roles in the U.S, as part of their ongoing expansion.
Essentially this person would manage and overall lead the projects surrounding procedural documents.
It is crucial you will therefore have experience in designing & developing standard operation processes & leading the technical writing within the regulatory (and further, cross-functional) framework.
Further to that...
> At least 8+ years experience with the majority of that in a technical writing role - there is flexibility for this role to be more senior than this
> Someone who understand the clinical, regulatory and PV landscape (GCP & GVP)
> A strong track record of working with regulatory, clinical & quality assurance teams would be preferred
> Attention to detail is crucial to such a role
Interested? Speak with Thomas Hancox on 7162261610 or thomas.hancox@cpl.com/LinkedIn!
