Head of Medical Writing

Job title:

Head of Medical Writing

Company:

Warman O’Brien

Job description

Head of Medical Writing and Regulatory AffairsThe Head of Medical Writing and Regulatory Affairs provides a senior level of expertise and management for our client’s medical writing team.They will be responsible for the fulfilment of medical writing and regulatory activities, ensuring optimal allocation of medical writing and regulatory resources.This is a hybrid role in Central London. Applicants must be prepared to go on site 4 days per week.Responsibilities:

• Take full accountability of all medical writing and regulatory activities.
• Direct line management responsibilities for the Medical Writing team. You will be managing two employees
• Provide regulatory expertise to project teams on all aspects of the clinical trials process.
• Support the organisation and preparation of regulatory submissions, ensuring accuracy and regulatory appropriateness.
• Oversee the preparation, and submission, of all clinical study documentation in accordance with regulatory requirements.
• Establish and maintain excellent sponsor relationships.

Required experience:

• 5-10 years of experience authoring pharmaceutical regulatory documentation, across phases I-III
• Line management experience desired

Expected salary

£85000 per year

Location

London

Job date

Fri, 29 Nov 2024 23:04:59 GMT

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