Regulatory Writer in United Kingdom
Meet Life Sciences is looking for an Regulatory Writer in United Kingdom
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
- Investigator brochures (IBs)
- Clinical trial authorisation (CTA) documents
- Patient narratives
BENEFITS
- Unlimited Holiday Policy (including office closure between Christmas and New Years)
- Bonus scheme
- Healthcare
- Pension
- Flexible working hours
- Extensive training development
Extra information
- Status
- Open
- Education Level
- Secondary School
- Location
- United Kingdom
- Type of Contract
- Part-time jobs
- Published at
- 04-07-2025
- Full UK/EU driving license preferred
- No
- Car Preferred
- No
- Must be eligible to work in the EU
- No
- Cover Letter Required
- No
- Languages
- English
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