Senior Medical Writer (Hybrid) – Global Regulatory Docs

Metronomia Clinical Research GmbH; United Kingdom; Hybrid; GBP 60,000 - GBP 80,000; Full time

Job summary

A clinical research organization based in the UK is seeking a Senior Medical Writer. In this role, you will author and finalize clinical documentation, manage timelines, and ensure high-quality outputs. The ideal candidate will have a degree in life sciences and experience in regulatory document preparation. The position offers a hybrid working model with competitive salary and benefits. Join a motivated team where your contributions are valued and recognized.

Benefits

Hybrid working models

Attractive remuneration

Comprehensive company benefits

Opportunities for training

Qualifications

• Strong understanding of drug development and clinical trials.
• Proven track record delivering submission-grade regulatory documents.
• Mastery of relevant ICH and regional guidance.

Responsibilities

• Plan, author, and finalize clinical and regulatory documents.
• Translate statistical outputs into compliant narratives.
• Drive document quality control and proofreading.
• Coordinate, collect, and compile source materials.
• Manage timelines, reviews, and comment reconciliation.

Skills

Excellent written and oral English

Attention to detail

Time management

Solution-oriented communication

Education

Degree in life sciences, public health, or related field

Job description

A clinical research organization based in the UK is seeking a Senior Medical Writer. In this role, you will author and finalize clinical documentation, manage timelines, and ensure high-quality outputs. The ideal candidate will have a degree in life sciences and experience in regulatory document preparation. The position offers a hybrid working model with competitive salary and benefits. Join a motivated team where your contributions are valued and recognized.