Preclinical Scientific Writer

7 days ago


Welwyn Garden City, United Kingdom 360technology s.r.l. Full time

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 Overview Our longstanding client, an innovative global organisation operating at the forefront of scientific research and therapeutic development, seeks a Preclinical Scientific Writer. 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 a globally renowned company 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 Call to Action 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, please apply to this Preclinical Scientific Writer role below or call Chloe McCausland on 01273 063769 between 8:30am - 5:00pm. #J-18808-Ljbffr



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