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Principal Regulatory Writer

3 months ago


London, Greater London, United Kingdom Vivify Talent Full time

Job Opportunity:
Principal Regulatory Writer (Remote)

About Us:
We are a dynamic and growing medical communications agency committed to excellence in pharmaceutical communications.

As we expand our clinical/regulatory department, we are actively seeking a talented and experienced Principal Regulatory Writer to join our team.


Role Overview:


As a Principal Regulatory Writer, you will play a pivotal role in translating complex scientific and clinical data into compelling regulatory documents.

Your expertise will be crucial in ensuring compliance with European regulations and industry standards.

Key Responsibilities:

nRegulatory Expertise:
Leverage your in-depth knowledge of European regulations to contribute to the development of high-quality regulatory documents, including but not limited to clinical study reports, regulatory submissions, protocols, investigator brochures, and marketing authorization applications

nTechnical Mastery:


Dive into the technical details of scientific and clinical data, demonstrating a keen ability to synthesize and present information accurately and coherently.

Stay abreast of industry advancements and regulatory updates to ensure the highest standards of technical accuracy.

nCollaborative Engagement:
Work collaboratively with cross-functional sponsor teams, bridging the gap between regulatory affairs, clinical teams, and other stakeholders. Your effective communication skills will be instrumental in fostering productive partnerships.

Flexible Working Arrangements:

nRemote Accessibility:
Embrace the opportunity to work remotely, allowing you to cultivate a conducive work environment that optimizes your productivity and work-life balance

nFull or part-time:
We are happy to consider writers for either part or full-time vacancies

Qualifications and Experience:

nBachelor's degree in a relevant scientific discipline.nProven experience in regulatory writing, with a focus on European regulations.nStrong technical acumen with the ability to comprehend and articulate complex scientific and clinical information.


Benefits:

nCompetitive compensation package reflective of your skills and expertise.nOpportunity for professional growth within a thriving SME environment.nFlexible working arrangements to accommodate your unique work style.


How to Apply:
Please apply directly through this advert, reach out to Vivify Talent via our website ( or on