Regulatory Writer (Senior / Principal)
EPM is partnered with a leading Medical Communications Agency to support a number of projects as they expand their Regulatory Writing team. They are currently looking for a Regulatory Writer (Senior/Principal level). See summary below:
Project Overview
- Project Type: Regulatory Writing (Submissions)
- Location: United Kingdom (Fully Remote)
- Contract Type: Permanent, Full-Time
- Ideal Start Date: Immediately
- Language Requirements: English
Key Responsibilities
- Transform complex scientific, clinical, and regulatory data into clear, precise, and audience appropriate documentation.
- Partner with cross functional teams to develop cohesive, scientifically robust narratives that support regulatory strategy and advance innovative medical science.
- Ensure all deliverables meet applicable regulatory requirements, industry guidelines, and internal quality standards.
- Conduct in depth research and maintain up to date knowledge of emerging scientific, clinical, and regulatory developments in relevant therapeutic areas.
- Develop high quality scientific, educational, and occasionally promotional materials that support the communication and adoption of next generation therapies worldwide.
Requirements
- A minimum of 18 months' experience as a medical writer within a Medical Communications agency or similar scientific writing environment.
- Demonstrated excellence in scientific writing, with a passion for transforming complex concepts into clear, engaging, and accurate content that meets stakeholder needs.
- Exceptional attention to detail and proven ability to synthesize and communicate intricate information for diverse audiences.
- A proactive learner who stays informed about evolving scientific, clinical, and industry trends.
- Energized by collaborative work and thrives in a fast paced, dynamic, and team oriented environment.
If this role is of interest to you, please apply directly to learn more. If not, feel free to share with your network.
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