Senior Regulatory Affairs CMC Consultant
Senior Regulatory Medical Writer - Cheshire/Switzerland
I'm currently seeking a Senior Regulatory Medical Writer on behalf of a well-established, independently run Medical Communications Agency to be located at either their Swiss or Cheshire offices. Renowned for their high levels of employee satisfaction, this organization encourages an open structure, entrepreneurial spirit and offers a diverse portfolio of projects. Flexible hours, competitive remuneration package and the possibility of home working is also available for the right candidate.
As a Senior Medical Writer, your responsibilities will include:
*Projects across a variety of therapeutic disciplines; coordinating and managing deadlines with multifunctional project teams
*Writing and editing regulatory documents, including protocols, study reports and submission dossiers
*Working in direct contact with clients to negotiate timelines, budgets and project specification
*Being involved in mentoring Junior staff, with the option of leading a small team
*Assisting in developing strategy and contributing ideas to help promote portfolio growth and company success
The ideal candidate will possess:
*A minimum of 3 years' experience in regulatory medical writing in the pharmaceutical industry, with ideally some exposure to a medical communications environment
*PhD/MD in medicine, pharmacy, life or health sciences
*Excellent command of the English language, both written and spoken; multilingual capabilities are desirable.
*Willing to travel to client meetings
If you're ready to learn new skills, experience novel fields and develop career-enhancing responsibility, find out further details by calling Emilie Francis on 0121 616 3477 for an informal chat. To apply, email CVs to EFrancis@pararecruit.com.
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