Responsible for developing procedural documents in collaboration with Subject Matter Experts (SMEs) in Global Drug Safety including:
- Meet with the SMEs to determine the process and the status of the existing procedure
- Develop plan for the revision to the document
- Make requested updates to the procedure
- Circulate drafts to the SMEs and stakeholders for review. Incorporate changes. Mediate discussions on conflicting requests.
- Review procedures for formatting and grammer errors as well as for clarity and accuracy
- Assist SME with collecting feedback on draft procedure and collecting documentation of approvals
- Potentially draft high level messages useful for training and communication on each procedure
All your information will be kept confidential according to EEO guidelines.