Associate Regulatory Affairs

CK Group have an opportunity for a Senior Associate in Regulatory Affairs, to join a global pharmaceutical company on a 12-month contract basis., * Execute the regional regulatory strategy and regional regulatory plans.

• Prepare supportive documentation for regulatory deliverables, including the management of clinical trial applications, marketing authorisations, and lifecycle management activities.

• Build effective relationships and communication paths across local and functional organizations.

• Master s degree (scientific area) OR Bachelor s degree (scientific area) and 2 years of directly related experience.

• Degree and in-depth regulatory experience and/or related to the region.

• Depth knowledge of regional countries legislation and regulations relating to medicinal products.

• Experience with Market Authorisations.