Senior Regulatory Medical Writer

• At least 3 years of relevant experience in writing study-related and submission-related clinical and regulatory documents.
• Prepare a variety of clinical regulatory documents as the lead writer in collaboration with members of client authoring teams and supported by other writers, as appropriate.
• Experience in writing Common Technical Document (CTD) modules, such as m2.5 Clinical Overview and m2.7s CTD summaries, and responding to Health Authority queries.
• Leadership in delivering individual documents, setting clear expectations for timelines and quality.
• Be responsible for providing document-specific advice to clients.
• Project manage the timelines and review cycles of your documents.
• Work in the client's regulatory document management systems.

Job Title: Senior Regulatory Medical Writer

Location: London, UK

Rate/Salary: .00 GBP Yearly

Job Type: Permanent

Trading as Aerotek. Allegis Group Limited, Maxis 2, Western Road, Bracknell, RG12 1RT, United Kingdom. No Allegis Group Limited operates as an Employment Business and Employment Agency as set out in the Conduct of Employment Agencies and Employment Businesses Regulations 2003. Aerotek and Actalent Services are companies within the Allegis Group network of companies (collectively referred to as "Allegis Group"). Aerotek, Actalent Services, Aston Carter, EASi, Talentis Solutions, TEKsystems, Stamford Consultants and The Stamford Group are Allegis Group brands. If you apply, your personal data will be processed as described in the Allegis Group Online Privacy Notice.

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