Senior Medical Writer

SENIOR MEDICAL WRITER

You will be fluent in English and eligible to work in Switzerland. The ideal candidate will join a growing team/company for international projects with a strong focus on quality communication.

This role will include various responsibilities:

* Writing/Editing/Reviewing scientific, clinical and/or regulatory documentation
.Collaborating with the team and other collaborators, partners as well as maintaining qualitative collaboration with clients
.Being experienced with regulations guidelines and authorities (EMA, FDA,).
.Communicate internally in regards to all potential issues, urgent projects and important updates
.Building and maintaining regulatory support to Medical Writing team & across functional units
.Assisting in the development and training of Junior Medical Writers if required
.Contributing to help Management to assess functional operations and plan for new procedures
.Participating in client meetings, preparing all documents or presentations needed, prioritising and planning of workload

Please be aware of the following requirements as an essential part of your profile:

*Fluency in English is essential -Great communication skills and team spirit needed.
.Experience or demonstrated abilities in Medical communication/Scientific writing (clinical and/or regulatory documents)
.Strong data analysis capabilities and a scientific mindset
.Regulatory awareness and experience with ICH and international authorities
.You possess A Scientific Degree (Master's, PhD, PharmaD, MD, MA)
.Rigorously project oriented - You are rigorous and pay attention to details
.You may have developed your expertise in academic, R&D, pre-clinical, clinical and regulatory environment within a CRO or pharmaceutical environmentMichael Bailey International is acting as an Employment Business in relation to this vacancy.