Sr. Regulatory Affairs Writer, Remote in the UKNonStop Consulting

TN United Kingdom; England; Remote; GBP 45,000 - 70,000; Full time

Job summary

An established industry player is seeking a Senior Regulatory Affairs Writer for a fully remote role in the UK. This position offers a stimulating work environment at the forefront of medical research, where you will write and edit critical regulatory documents while mentoring a team. You will have the opportunity to collaborate across functions, ensuring accuracy and compliance in submissions. With a competitive compensation package and professional growth opportunities, this is a chance to advance your career in a dynamic field. If you're passionate about contributing to medical science, apply now!

Benefits

Competitive Compensation Package

Professional Growth Opportunities

Stimulating Work Environment

Qualifications

• 5+ years of experience in regulatory affairs writing.
• Strong background in life sciences required.

Responsibilities

• Write and edit clinical regulatory documents for submissions.
• Lead outsourced writing deliverables and ensure compliance.
• Collaborate in a cross-functional environment.

Skills

Regulatory Affairs Writing

Clinical Document Writing

Problem Solving

Cross-Functional Collaboration

Education

PhD in Life Sciences

Master's Degree in Life Sciences

Job description

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Sr. Regulatory Affairs Writer, Remote in the UKNonStop Consulting, england, uk

Client:

NonStop Consulting

Location:

England, UK, United Kingdom

Job Category:

Other

EU work permit required:

Yes

Job Reference:

1977ad4943c2

Job Views:

9

Posted:

26.04.2025

Expiry Date:

10.06.2025

Job Description:

Are you an experienced regulatory affairs writer looking for a new challenge? Our client, a top medical devices company, is seeking a Senior Regulatory Affairs Writer to join their dynamic team. This fully remote role offers a stimulating work environment at the forefront of medical research, with opportunities for professional growth and development. You can work from anywhere in the UK, Israel, or Germany.

Responsibilities:

• Write and edit clinical regulatory documents: CSRs, IBs, Protocols, Summaries, Briefing Books, Pediatric Plans, and Model 2 summaries for submissions. Your expertise in project consensus and issue anticipation will be highly valued.
• Oversee and mentor: Lead outsourced writing deliverables, provide guidance, support, and strategic assistance to the team, ensuring accuracy and regulatory compliance.
• Collaborate and communicate: Work effectively in a cross-functional environment, communicating clearly and driving project consensus.

Requirements:

• Life sciences background: PhD/PharmD with at least 5 years of experience or Master’s degree with at least 7 years of experience.
• Willingness to learn and grow: Eagerness to develop skills and contribute to the team’s success.
• Problem-solving skills: Ability to anticipate issues, drive consensus, and find solutions.

Benefits include a competitive compensation package, professional growth opportunities, and a stimulating work environment at the forefront of medical research. Join us and contribute to advancing medical science!

Apply now by sending your CV in Word format or sharing it directly. This is a 1-year contract, with an immediate start preferred. Forward your application to Oksana at [emailprotected] or via LinkedIn.

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