REGULATORY AFFAIRS Analyst Consultant
Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says it’s the best of both worlds….
ClinChoice is searching for a Regulatory Affairs Associate Consultant for 12 months Contract with possibility of extension to join one of our clients.
ClinChoice is a global full-service CRO with a strong focus on quality, professional development, and supportive culture. As a client-facing role, we are looking for confident candidates with the ability to work independently whilst establishing a high-trust environment with the client’s counterparts.
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Job Title |
ANALYST REGULATORY AFFAIRS Consultant |
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Job Summary |
Ensures proper submission and approvals for market licenses including new registrations, changes and timely renewals, and establishment registrations, organizing and balancing a multitude of projects simultaneously. |
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Scope |
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Major Roles and Responsibilities |
· Support projects as representative of the subject/country. · Elaborate procedures of the area. · Organize team meetings and elaborate agenda and minutes. · Manage quality issues. · Manage compulsory certification (INMETRO) and GMP activities. |
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Competencies |
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GLP Behaviors |
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Experience/ Qualification Requirements |
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Education Requirements |
· A Bachelor’s Degree in Engineering, Pharmacy or other life science: Can be a person with related experience and/or training or equivalent combination of education and experience. Advanced reading and writing Skills in English are required; intermediate to advanced speaking is desirable. Fluent in Portuguese.
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