Senior Medical Writer — Remote Lead for Regulatory Documents

ICON Strategic Solutions; United Kingdom; On-site; GBP 50,000 - 70,000; Full time

Job summary

A global healthcare organization is seeking a Senior Medical Writer to play a key role in developing medical writing strategies for clinical research. The candidate will produce essential regulatory documents and work closely with a leading pharma company to ensure high-quality deliverables. This position emphasizes strong writing skills, regulatory knowledge, and collaboration within a dynamic team environment. Competitive salary and benefits are offered, promoting well-being and work-life balance.

Benefits

Various annual leave entitlements

Health insurance offerings

Retirement planning

Global Employee Assistance Programme

Flexible optional benefits

Qualifications

• 3-5 years of experience in medical writing in the pharmaceutical or CRO industry.
• Ability to convert scientific data into clear and structured messages.
• Experience in leading document creation and coordination of authoring functions.

Responsibilities

• Independently produce clinical and regulatory documents.
• Analyze and interpret data for document composition.
• Act as the primary contact for study teams regarding document preparation.

Skills

Strong writing skills

Data analysis

Document preparation

Knowledge of regulatory documents

Education

Advanced degree in Life Sciences, Pharmacy, or Medicine

Bachelor's degree minimum

Job description

A global healthcare organization is seeking a Senior Medical Writer to play a key role in developing medical writing strategies for clinical research. The candidate will produce essential regulatory documents and work closely with a leading pharma company to ensure high-quality deliverables. This position emphasizes strong writing skills, regulatory knowledge, and collaboration within a dynamic team environment. Competitive salary and benefits are offered, promoting well-being and work-life balance.