Senior Medical Writer & Regulatory Submissions Lead

BioMarin; Greater London; On-site; GBP 60,000 - 75,000; Full time

Job summary

A global biotechnology company in the UK is seeking a Senior Medical Writer to manage the preparation of clinical study documents and ensure compliance with regulatory submissions. This role requires advanced medical writing experience, excellent communication skills, and a strong understanding of drug development processes. The successful candidate will collaborate with cross-functional teams and lead document preparation efforts to support impactful medical writing initiatives.

Qualifications

• Experience in preparing regulatory submissions.
• Strong understanding of drug development processes.
• Ability to collaborate with cross-functional teams.

Responsibilities

• Manage preparation of clinical study documents.
• Ensure compliance with regulatory submissions.
• Lead document preparation efforts for various projects.

Skills

Advanced medical writing experience

Excellent communication skills

Regulatory knowledge

Job description

A global biotechnology company is seeking a Senior Medical Writer to manage the preparation of clinical study documents and ensure compliance with regulatory submissions. This role requires advanced medical writing experience and a strong understanding of drug development processes. The position involves collaboration with cross-functional teams and the ability to lead document preparation efforts. Ideal candidates will possess excellent communication skills and regulatory knowledge to support impactful medical writing efforts.