As a Document Specialist with experience in the pharmaceutical industry you have the opportunity to join a renowned global pharmaceutical company while supporting the management of internally generated protocols, reports & documents during the drug development life cycle. The ideal candidate can effectively work independently and is proficient in report formatting & document publishing.
Document Specialist Minimum Qualifications:
B.S. in scientific or technical field (biology, chemistry, etc.)
1-3+ years of pharmaceutical or healthcare experience
Experience with data review, report formatting & document polishing
Document management experience in the pharmaceutical industry
Process characterization/development experience or a specialty in drug development
Responsibilities:
Formatting, editing, and publishing of internal nonclinical protocols, reports and documents during the entire drug development life cycle
Ability to review & check documents with high attention to detail & accuracy
Compile & analyze data to create data tables for campaign summary & VC reports
Manage & organize team's SharePoint site
What's In It For You:
The opportunity to join a global, renowned Pharmaceutical company