Expert Specialist - Global Scientific Communications - Regulatory
Eli Lilly
Little Island, Ireland
Not specified; not specified; benefits include hea...
Hybrid
1 year clinical research experience
1 year editing and proofreading skills
Document control and workflow systems knowledge
Eli Lilly is seeking an Expert Specialist in Global Scientific Communications within their Regulatory team in Little Island, Ireland. The role focuses on managing regulatory document processes and ensuring compliance, while offering a supportive and inclusive work environment with a range of benefits
Job Summary
The role supports the delivery of Global Scientific Communications regulatory documents through comprehensive planning, tracking, and compliance activities.
Eli Lilly Cork offers a premium workspace with flexible hybrid working options, healthcare benefits, pension, life assurance, and onsite amenities including a gym and canteen.
This position requires maintaining proficiency in software tools like Documentum and Datavision while ensuring all regulatory documents meet strict guidelines and internal policies.
Matching Summary
Match Score: 85
Eli Lilly is seeking an Expert Specialist in Global Scientific Communications within their Regulatory team in Little Island, Ireland. The role focuses on managing regulatory document processes and ensuring compliance, while offering a supportive and inclusive work environment with a range of benefits.
Salary
Not specified; Not specified; Benefits include healthcare, pension, life assurance, subsidised canteen, onsite gym, travel subsidies, and on-site parking
Skills & Requirements
Must-have
1 year clinical research experience
1 year editing and proofreading skills
Document control and workflow systems knowledge
Regulatory document submission process expertise
Project management for regulatory deliverables
Nice-to-have
Creative problem-solving abilities
Cross-cultural collaboration skills
Experience with medical publication databases
Ability to work independently in a team
Strong organizational and record management
Key Requirements
1 year of clinical research or pharmaceutical industry experience
Associate's or Bachelor's degree preferred
Demonstrated command of English grammar and editing techniques