Principal Regulatory Writer

Principal Regulatory Writer

Edinburgh Full-Time 48000 - 72000 £ / year (est.) No home office possible
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At a Glance

  • Tasks: Join our team as the first Medical Writer, creating clinical documents.
  • Company: We're a specialty pharmaceutical company focused on innovative solutions.
  • Benefits: Enjoy fully remote work and flexible hours.
  • Why this job: Be a pioneer in our writing team and impact patient care.
  • Qualifications: Experience with clinical documents is essential; strong writing skills required.
  • Other info: This is a unique opportunity to shape our regulatory writing process.

The predicted salary is between 48000 - 72000 £ per year.

Fully Remote role Job Summary Making sure you fit the guidelines as an applicant for this role is essential, please read the below carefully. We are a specialty pharmaceutical company looking for a Principal Medical Writer to join our team as our first Medical Writer and partner closely with clinical and regulatory teams. The ideal candidate would have worked with a broad range of clinical documents. This role can be home based anywhere. Job Overview Who are we: We are a specialty pharmaceutical company with … JBLK1_UKTJ

Principal Regulatory Writer employer: Vivify Talent Limited

As a fully remote specialty pharmaceutical company, we pride ourselves on fostering a collaborative and innovative work culture that empowers our employees to thrive. We offer competitive benefits, including flexible work hours and opportunities for professional development, ensuring that our team members can grow their skills while contributing to meaningful projects. Join us to be part of a pioneering team where your expertise as a Principal Regulatory Writer will directly impact patient outcomes and drive our mission forward.
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Contact Detail:

Vivify Talent Limited Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Principal Regulatory Writer

✨Tip Number 1

Familiarize yourself with the specific types of clinical documents that are commonly used in the pharmaceutical industry. This knowledge will not only help you understand the role better but also allow you to speak confidently about your experience during the interview.

✨Tip Number 2

Network with professionals in the regulatory writing field. Engaging with others who have similar roles can provide insights into the expectations and challenges of the position, which can be invaluable during your discussions with us.

✨Tip Number 3

Prepare to discuss your experience collaborating with clinical and regulatory teams. Highlighting specific examples of successful partnerships will demonstrate your ability to work effectively in a cross-functional environment.

✨Tip Number 4

Stay updated on the latest regulations and guidelines in the pharmaceutical industry. Showing that you are proactive about your professional development will impress us and indicate that you are serious about the role.

We think you need these skills to ace Principal Regulatory Writer

Medical Writing
Regulatory Knowledge
Clinical Document Preparation
Attention to Detail
Strong Communication Skills
Project Management
Ability to Work Independently
Understanding of Clinical Trials
Knowledge of FDA and EMA Regulations
Editing and Proofreading Skills
Collaboration with Cross-Functional Teams
Time Management
Adaptability to Changing Guidelines
Technical Writing Skills

Some tips for your application 🫡

Understand the Role: Make sure to thoroughly read the job description for the Principal Regulatory Writer position. Understand the specific requirements and responsibilities, especially regarding clinical documents.

Highlight Relevant Experience: In your application, emphasize your experience with clinical writing and regulatory submissions. Provide specific examples of documents you have worked on that align with the role's expectations.

Tailor Your CV: Customize your CV to reflect the skills and experiences that are most relevant to the position. Use keywords from the job description to ensure your application stands out.

Craft a Compelling Cover Letter: Write a cover letter that not only outlines your qualifications but also expresses your enthusiasm for the role and the company. Mention why you are particularly interested in working with this specialty pharmaceutical company.

How to prepare for a job interview at Vivify Talent Limited

✨Understand the Role

Make sure you have a clear understanding of what a Principal Regulatory Writer does. Familiarize yourself with the types of clinical documents you will be expected to work on and how they fit into the regulatory process.

✨Showcase Your Experience

Prepare to discuss your previous experience with clinical documents in detail. Highlight specific projects where you contributed significantly, especially those that involved collaboration with clinical and regulatory teams.

✨Demonstrate Communication Skills

As a Principal Medical Writer, effective communication is key. Be ready to provide examples of how you've successfully communicated complex information to various stakeholders in the past.

✨Ask Insightful Questions

Prepare thoughtful questions about the company's processes, team dynamics, and expectations for the role. This shows your genuine interest in the position and helps you assess if it's the right fit for you.

Principal Regulatory Writer
Vivify Talent Limited
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  • Principal Regulatory Writer

    Edinburgh
    Full-Time
    48000 - 72000 £ / year (est.)

    Application deadline: 2026-12-21

  • V

    Vivify Talent Limited

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