Senior/Principal Medical Editor – FSP. Syneos Health is a leading fully integrated life sciences services organization dedicated to accelerating customer success across the drug development and commercialization continuum. Our Clinical Solutions team brings deep editorial expertise to understand customer needs and translate them into effective solutions. Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with problem solvers to deliver results that matter for patients. This is a remote opportunity based in the United Kingdom. Responsibilities: - Maintain familiarity with FDA, EU, and other relevant guidelines to ensure documents meet sponsor and regulatory requirements. - Represent the editorial group on study teams and cross-departmental projects. - Monitor timelines and budgets, and inform leadership if deliverables are at risk. - Provide technical support, mentorship, and training to medical editors; advise on quality review and editorial standards. - Lead complex or large medical writing projects, coordinating meetings and requirements. - Copyedit documents according to AMA style and internal guidelines. - Perform quality reviews to ensure accuracy. - Contribute to process improvements and updates to internal policies. - Manage projects in line with medical writing SOPs and client standards, on time and on budget. This role offers the opportunity to work with a global team and contribute to the development and regulatory submission processes.

Senior/Principal Medical Editor – FSP. Syneos Health is a leading fully integrated life sciences services organization dedicated to accelerating customer success across the drug development and commercialization continuum. Our Clinical Solutions team brings deep editorial expertise to understand customer needs and translate them into effective solutions. Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with problem solvers to deliver results that matter for patients. This is a remote opportunity based in the United Kingdom. Responsibilities: - Maintain familiarity with FDA, EU, and other relevant guidelines to ensure documents meet sponsor and regulatory requirements. - Represent the editorial group on study teams and cross-departmental projects. - Monitor timelines and budgets, and inform leadership if deliverables are at risk. - Provide technical support, mentorship, and training to medical editors; advise on quality review and editorial standards. - Lead complex or large medical writing projects, coordinating meetings and requirements. - Copyedit documents according to AMA style and internal guidelines. - Perform quality reviews to ensure accuracy. - Contribute to process improvements and updates to internal policies. - Manage projects in line with medical writing SOPs and client standards, on time and on budget. This role offers the opportunity to work with a global team and contribute to the development and regulatory submission processes.