Proclinical is seeking a Senior Manager, Medical Writing. This role will work closely alongside the project teams to create and maintain clinical documents, ensuring compliance with regulations and standards. The successful candidate will also oversee contract writers and contribute to the planning and resourcing of writing deliverables.

Responsibilities:

Produce high-quality writing deliverables on time.Plan, write, edit, and format key clinical documents independently.Manage the review and finalization process for documents.Represent Medical Writing on project teams and collaborate with the Director of Medical Writing.Work effectively with various internal and external stakeholders.Serve as a subject matter expert for clinical document production.Contribute to the development and maintenance of SOPs and templates.

Key Skills and Requirements:

Bachelor's degree in Life Science or English/Communications with relevant expertise.Experience as a medical writer, preferably with regulatory submissions.Knowledge of Good Clinical Practices, FDA regulations, and the drug development process.Ability to manage multiple projects in a fast-paced environment.Strong attention to detail and timely completion of assignments.Proficiency in Microsoft Windows, Word, Excel, and PowerPoint.Ability to travel approximately 10%.

If you are having difficulty in applying or if you have any questions, please contact Jake Robinson at j.robinson@proclinical.com

Apply Now:

If you are interested in learning more or applying to this exciting opportunity, please complete the form below and attach a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist, please request a call back at the top of this page.

Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Proclinical is acting as an Employment Agency in relation to this vacancy.