Senior Regulatory Medical Writer

Role: Senior Regulatory Medical WriterLocation: Hybrid - WelwynHours: Full-timePay: £45.50 - £56.40 per hour PAYE basic excluding holiday pay or £60 - £75 per hour LTD/UMBContract: 12-Month Contract (Outside IR35)An excellent opportunity has arisen for a Senior Regulatory Medical Writer to join one of our longstanding global pharmaceutical clients.This senior-level role will focus on developing regulatory content strategies and delivering high-quality clinical, safety and medical device documentation for global submissions. The successful candidate will work independently, lead cross-functional contributors and help shape submission content throughout the product lifecycle.Benefits:25 days holiday + bank holidays12-month contract outside IR35Hybrid working based in WelwynFree, on-site parkingOpportunity to support global regulatory submissionsExposure to pharmaceutical and medical device programmesSenior-level strategic and cross-functional responsibilityThe Requirements:Degree in Life Sciences or an equivalent scientific disciplineAt least 5 years of relevant experience within the pharmaceutical or biotechnology industryStrong medical and regulatory writing experienceExperience independently managing complex regulatory writing projectsExperience producing clinical protocols and pharmacovigilance documents, including DSURs and PBRERsStrong understanding of clinical, safety and medical device regulatory documentationFamiliarity with drug and device development regulations, ..... full job details .....