Regulatory Writer

JR United Kingdom; North East; Remote; GBP 40,000 - 60,000; Full time

Job summary

A leading company in the life sciences sector is seeking a Regulatory Writer to provide high-quality regulatory documentation. This remote role involves authoring and reviewing essential documents to meet regulatory compliance and client expectations, along with managing concurrent projects efficiently.

Benefits

Unlimited Holiday Policy

Qualifications

• Experience in regulatory writing and understanding regulatory authority expectations.
• Ability to juggle multiple projects efficiently.

Responsibilities

• Author regulatory documents across various therapeutic areas.
• Review client-supplied materials critically.
• Collaborate directly with clients to manage timelines.

Skills

Regulatory documentation

Attention to detail

Communication

Project management

Critical review

Job description

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Regulatory Writer, newcastle-upon-tyne, tyne and wear

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Client:

Meet Life Sciences

Location:

newcastle-upon-tyne, tyne and wear, United Kingdom

Job Category:

Other

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EU work permit required:

Yes

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Job Views:

2

Posted:

26.06.2025

Expiry Date:

10.08.2025

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Job Description:

Regulatory Writer - remote

PRIMARY PURPOSE OF THE ROLE

To provide high-quality, concise, and accurate regulatory documentation that meets the expectations of both clients and regulatory authorities.

CORE RESPONSIBILITIES

• Author regulatory documents across various therapeutic areas, ensuring outputs are clear, factual, scientifically accurate, and free from over-interpretation.
• Adhere to established standard operating procedures and regulatory processes provided by clients.
• Demonstrate a foundational understanding of the expectations of regulatory authorities for submissions.
• Review client-supplied materials critically, including protocols, statistical analysis plans (SAPs), data listings, templates, and style guidelines.
• Assess documentation quality, data integrity, and project resource use—taking prompt action where issues are identified.
• Conduct accurate data checks of documents created by peers to ensure consistency and quality.
• Perform literature searches using publicly available or commercial databases to verify citations, locate references, and gather background context or regulatory precedent.
• Collaborate directly with clients to manage timelines and address emerging issues.
• Juggle multiple concurrent projects efficiently while meeting deadlines and maintaining quality standards.
• Proactively notify team members of risks or potential problems.
• Communicate clearly and professionally with internal team members and external contacts.
• Deliver work on time and within agreed-upon budgets.
• Follow internal and client-aligned procedures consistently.
• Contribute to additional duties as reasonably required to support project or business needs.

CORE DELIVERABLES

• Produce a wide range of documents, which may include (but are not limited to):
• Clinical study protocols
• Clinical study reports (CSRs)
• Executive summaries
• Common Technical Document (CTD) clinical summaries
• Clinical trial authorisation (CTA) documents

BENEFITS

• Unlimited Holiday Policy (including office closure between Christmas and New Years)