SE trainee SIVP:
The S Tunisia learner will be responsible for the post-approval changes dossier evaluation, preparation and dispatch to the countries for submission in line with local regulations and planning set up by Global/Regional BU/Country regulatory team.
Specific requirements and responsibilities include:
and /or any type of response documents to the Health Authorities questions by interacting with the relevant stakeholders (BU region regulatory, GRA, RSO local medical, local Pharmacovigilance department etc.) and monitoring of dossiers dispatch up to submission.
Foster an environment/culture of learning and sharing of best practice within the team
Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.
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