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