Key skills
RChange ManagementCommunication
About this role
Role Overview
- Oversee clinical labelling content compliance for clinical supplies across R&D
- Collaborating closely with clinical supply chain, packaging, IT technology, quality, and third-party teams
- Shape processes and facilitate effective decision-making
- Support audits and inspections
- Accountable for management and oversight of GSK’s preferred third-party partner(s)
- Respond to queries from Regulatory Authorities on label content
Requirements
- Degree or relevant experience in life sciences, pharmacy, regulatory, quality, or similar discipline
- Demonstrated experience in clinical trial labelling, pharmaceutical labelling, or clinical trial supply operations
- Expert in GMP for Clinical Trial Labelling
- Strong attention to detail
- Adept project and change management skills
- Demonstrated ability to set and reach goals
- Strong written and oral communication skills
- Proficiency with technology and IT systems used in clinical trial labels
Benefits
- Competitive salary
- Annual bonus based on company performance
- Healthcare and wellbeing programmes
- Pension plan membership
- Shares and savings programme
- Hybrid working model