Senior Science
Pubblicato il 21-09-2026 - Altro in Italia
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Standard (Mon-Fri)
Environmental Conditions
Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner, and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development, and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future.
We are excited to be expanding our Medical Writing FSP Team in Europe. experience in Structured Content Authoring systems and automation to support delivery would be preferred.
We are seeking a talented and experienced Senior Medical Writer to join our team. The Senior Medical Writer will be responsible for developing high-quality clinical and regulatory documents, ensuring they meet all regulatory requirements and company standards.
Write and edit clinical and regulatory documents, including clinical study reports, protocols, investigator brochures, and regulatory submissions.
Collaborate with cross-functional teams to gather necessary information and ensure the accuracy and completeness of documents.
Manage timelines and deliverables for assigned projects.
Mentor and provide oversight to junior medical writers and ensure high-quality deliverables
Education and Experience
Bachelor's degree in a scientific discipline or equivalent and relevant formal academic / vocational qualification required; Advanced degree preferred.
Regulatory writing experience that provides the knowledge, skills, and abilities to perf