GlaxoSmithKline
Regulatory Medical Writing Expert
Job Description
Join GSK in Hertfordshire as a Regulatory Medical Writing Expert, where you'll manage complex regulatory projects in a hybrid working environment. Bring your clinical research and writing skills to this vital role.
As part of your role, you will be responsible for authoring high-quality regulatory documents including protocols and study reports. You will lead the planning and delivery of clinical dossier documents, ensuring adherence to quality standards and timelines. The position requires proficiency in statistical analysis, clinical data interpretation, and collaborating with multidisciplinary teams for optimal document development.
Key Responsibilities:
• Create high-quality clinical regulatory documentation
• Oversee global regulatory submissions process
• Collaborate to ensure compliance with GSK standards
• Manage multiple regulatory writing projects
• Review and improve data presentation in documents
Requirements:
• PhD or equivalent in life sciences<...
As part of your role, you will be responsible for authoring high-quality regulatory documents including protocols and study reports. You will lead the planning and delivery of clinical dossier documents, ensuring adherence to quality standards and timelines. The position requires proficiency in statistical analysis, clinical data interpretation, and collaborating with multidisciplinary teams for optimal document development.
Key Responsibilities:
• Create high-quality clinical regulatory documentation
• Oversee global regulatory submissions process
• Collaborate to ensure compliance with GSK standards
• Manage multiple regulatory writing projects
• Review and improve data presentation in documents
Requirements:
• PhD or equivalent in life sciences<...