You will represent the Publishing team on multidisciplinary project teams, and work closely with Regulatory colleagues to ensure timely submission of dossiers, including document formatting and quality control/assurance tasks on submissions. You will also provide on the job training in the publishing process when required.

Requirements

• You will have two years regulatory affairs experience of document management technology and electronic publishing software (Core dossier) gained in a pharmaceutical company or CRO
• You will have experience and a good knowledge of drug development and regulatory submission content and formats
• Bachelors degree in life sciences, pharmacy, nursing or RN, or equivalent clinical research experience.