Key skills
Communication
About this role
Role Overview
- Anchor references to promotional pharmaceutical materials within Veeva or other approval systems when provided with an offline reference pack
- Review existing reference anchors for accuracy and compliance with regulatory standards; update reference anchors for subsequent versions of materials
- Provide comprehensive editorial support as needed, including fact-checking and quality checking of copy and amendments to ensure accuracy and consistency
- Communicate progress and issues in a professional and timely manner to relevant stakeholders
- Maintain strict adherence to project deadlines and proactively manage workload priorities
Requirements
- Scientific and medical literacy
- demonstrates sufficient scientific/medical knowledge to check pharmaceutical claims in promotional materials are referenced accurately
- Regulatory compliance awareness
- understands pharmaceutical marketing approval processes and regulatory standards, with existing practical experience of using Veeva
- Attention to detail and quality assurance
- exhibits meticulous attention to detail when anchoring references and reviewing content
- Professional communication skills
- proactively and clearly communicates progress and work status
- Workload management and deadline adherence
- manages competing priorities effectively, maintaining strict adherence to project timelines while delivering consistent quality of output
- Team player
- enthusiastic and collaborative, with the desire to exceed objectives
Benefits
- Must be willing to work UK shift hours