Responsibilities
- 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
- Experience in Veeva and other pharmaceutical marketing approval systems
- Scientific or medical background sufficient for understanding, checking and referencing claims
- Diligent and proactive work ethic
- Ability to use initiative to check work quality
- Ability to identify and rectify or communicate errors effectively
