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.
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Prepare supportive documentation for regulatory deliverables, including the management of clinical trial applications, marketing authorisations, and lifecycle management activities.
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Build effective relationships and communication paths across local and functional organizations.
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Master s degree (scientific area) OR Bachelor s degree (scientific area) and 2 years of directly related experience.
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Degree and in-depth regulatory experience and/or related to the region.
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Depth knowledge of regional countries legislation and regulations relating to medicinal products.
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Experience with Market Authorisations.
Contact Detail:
The CK Group Inc Recruiting Team
