EPM Scientific is partnering with a leading global pharmaceutical company that is experiencing a surge in regulatory activity due to an exciting pipeline of new products. To support this growth, we are seeking experienced Regulatory Writers on a freelance basis.

Freelance Regulatory Writer - Global Pharmaceutical Company
Contract Length: 12 Months
Commitment: 20-40 Hours per Week
Location: 100% Remote
Start Date: ASAP
Compensation: Competitive, Hourly Rate (Negotiable)

Key Requirements:

• Minimum of 10 years of regulatory writing experience - essential
• Proven expertise in CTD Modules 2.7.1 and 2.7.2 - essential
• Strong background in authoring clinical safety summaries, protocols, and investigator brochures
• Ability to work independently and meet tight deadlines in a dynamic environment
• Previous experience working with large pharmaceuticals
• Professional/Fluent speaking and writing proficiency in English - essential
• Strong educational background in high sciences, preferably PhD