Oncology Regulatory Affairs Director
VirtualVocationsShreveport, Louisiana, United Statesjob_description.job_card.variable_hours_ago
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A company is looking for an Associate Director, Regulatory Affairs (Oncology).
Key Responsibilities
Manage regional regulatory activities as part of a Global Regulatory Team
Lead regulatory activities for assigned projects in alignment with global registration strategy
Plan, coordinate, and prepare regulatory submissions while ensuring compliance with global regulatory requirements
Required Qualifications
Bachelor's degree in a related field, preferably in a scientific discipline
At least 7 years of experience in the biopharmaceutical or pharmaceutical industry, with a minimum of 4 years in regulatory affairs
Oncology product development experience preferred
Experience with electronic regulatory submissions and regulatory templates
Understanding of EU Clinical Trial Regulation and ROW country regulatory requirements related to clinical trials
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Director Regulatory • Shreveport, Louisiana, United States
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