Are you ready to become a key stakeholder in a leading global pharmaceutical company's regulatory activities? Ready to feel valued and recognized at work? Looking to add more to your extensive experience?
THEN I HAVE THE OPPORTUNITY FOR YOU!
My client is looking for an Associate Director of Regulatory Affairs to join their company and manage worldwide interactions with Regulatory Agencies. As well as being a key member to teams responsible for evaluation of product concepts.
The opportunity allows you to develop and implement regulatory strategies to facilitate the progress of programs in development, provide any direction or solutions to teams, and manage all junior staff.
Review of protocols, reports and all regulatory documentation (CTA's, labelling, safety & efficiency) Ensure timely submissions of INDs/CTAs/IMPDs, MAAs/NDAs and variations for products Represent the company in external forum Provide training and regulatory intelligence to organization
Minimum of Bachelors/Masters in scientific discipline Minimum of 8 year's Regulatory Affairs experience Must currently reside in Sweden