Senior Regulatory & Scientific Writer - Pharma/Biotech

Pop Science; Greater London; Remote; GBP 60,000 - 80,000; Part time

Job summary

A leading regulatory consultancy in Greater London is seeking a freelance Senior Regulatory & Scientific Writer to join their team. The role involves producing high-quality regulatory documents for pharmaceutical and biotech products. Candidates should possess a degree in life sciences with a preference for advanced degrees, along with 10+ years of relevant experience in medical writing. Strong attention to detail, excellent communication skills, and familiarity with regulatory guidelines are essential for success in this role.

Qualifications

• Minimum 10+ years’ experience as a medical writer in a pharmaceutical, biotech, or CRO environment.
• Familiarity with drug development processes and regulatory submission requirements.
• Experience with clinical trial documentation and regulatory submissions.

Responsibilities

• Review, develop, write, and edit scientific and regulatory documents.
• Ensure compliance with regulatory requirements and internal standards.
• Participate in interpreting and planning data presentations.

Skills

Excellent written and verbal communication skills

Attention to detail

Ability to interpret complex scientific data

Education

Degree in life sciences (Biology, Pharmacology, Medicine)

Advanced degree (MSc, PhD, MD)

Tools

Microsoft Office Suite (Word, Excel, PowerPoint)

Job description

A leading regulatory consultancy in Greater London is seeking a freelance Senior Regulatory & Scientific Writer to join their team. The role involves producing high-quality regulatory documents for pharmaceutical and biotech products. Candidates should possess a degree in life sciences with a preference for advanced degrees, along with 10+ years of relevant experience in medical writing. Strong attention to detail, excellent communication skills, and familiarity with regulatory guidelines are essential for success in this role.