Role: Preclinical Scientific Writer
Location: Welwyn Garden City - Hybrid or Remote (flexible for the right candidate)
Hours: Full-time
Pay: £55.96 - £67.16 per hour PAYE basic (excluding holiday pay) OR £75 - £90 per hour UMB/LTD
12 Month Contract (Outside IR35) - with extension expected
An excellent opportunity has arisen for a Preclinical Scientific Writer to join one of our longstanding clients, an innovative global organisation operating at the forefront of scientific research and therapeutic development. This role sits within a highly collaborative documentation and regulatory writing function supporting preclinical and nonclinical submissions for global health authorities.
Fully remote or hybrid working is available for the right individual.
Benefits:
Remote or hybrid working flexibility
Weekly competitive pay (PAYE or UMB/LTD)
Generous holiday (25 days per annum + bank holidays)
Opportunity to support high-impact global regulatory submissions
Work within a scientific, collaborative, cross-functional environment for globally renowned company
The Requirements:
University degree in a life science field
Several years' experience in scientific writing within a preclinical, nonclinical or regulatory domain
Proven ability to prepare, write, edit, and coordinate regulatory documentation (e.g., IND, CTA, NDA, BLA, MAA submissions)
Strong command of writing and editing tools; comfortable adopting new technologies
Excellent communication and stakeholder management skills
Ability to take ownership, work proactively, and manage delivery timelines
High attention to detail and commitment to documentation quality
The Role:
Manage the preparation, review, and submission of preclinical/nonclinical summary documents for early development and global marketing applications
Collaborate with regulatory, scientific, and project leadership teams to ensure comprehensive and accurate dossiers are delivered
Compose and support the development of study reports, submission documents, and scientific content
Maintain and enhance documentation processes, tools, and guidelines to support high-quality output
Represent the preclinical writing function in global initiatives focused on process optimisation and technology improvements
Ensure all documents adhere to internal standards, ICH guidelines, and regulatory expectations
If you're keen to join an exceptional scientific team who can offer flexibility, innovation, and the opportunity to contribute to meaningful global development work, then please apply to this Preclinical Scientific Writer role below or call Chloe McCausland on 01273 063769 between 8:30am - 5:00pm .
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