Create documents for all phases of drug development, including manuscripts, abstracts, posters, oral presentations and slide sets through their lifecycle
Independently write first drafts with input from lead author from CSR and/or TFLs
Coordinate or complete journal/abstract submissions adhering to journal and congress requirements
Perform Project Management responsibilities including: managing specific details of a project, coordinating with the authors, scheduling and participating in meetings, showing excellent interpersonal skills and flexibility
Coordinate with lead author to prepare outlines and timelines
Manage and drive document reviews and address comments. Facilitate comment resolution discussions with internal client authors and external KOLs.
Obtain and retain required documentation for publication per client policies.
Understand and follow all client publication policies and procedures, including confidentiality, secure file transfer, copyright law and privacy protection
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