Only first 12 candidates will be reviewed. Requests will go on hold automatically once this limit has been reached. No additional slots will be allowed unless the HM needs additional profiles.

must have Veeva Vault RIM Publishing experience
Remote worker is ok
Provide Submission Management and Publishing support for Global Regulatory Affairs for submissions to US, EU and Canada.
Provide regulatory operations support for assigned projects.
Works in close collaboration with internal stakeholders and supports multiple projects.
Adherence to submission timelines and able to deliver high quality submissions
Ensures compliance with global regulatory requirements and adherence to internal policies and processes
Responds to regulatory requests from across the organization in a timely manner
Process payments in support of HA Submissions
Basic knowledge of medical device and pharma submission standards
Veeva Vault RIM application knowledge
Document Management Tools expertise (proficient in Excel, Word and Adobe Acrobat PRO)