Medical Writer - Regulatory
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
This is a fantastic opportunity to contribute to high-impact projects with a globally recognized organization, all from the comfort of your home.
If you meet the criteria and are ready to take on a new challenge, we encourage you to apply today!
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