Posted in General Business 30+ days ago.
Type: Full-Time
Location: Alameda, California
SUMMARY/JOB PURPOSE:
The Senior Regulatory Affairs Associate is responsible for managing and maintaining existing investigational new drug (IND) and clinical trial application (CTA) submissions and preparing amendments in compliance with guidelines and regulations. This individual coordinates, compiles, and tracks product applications to regulatory agencies.
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If you like wild growth and working with happy, enthusiastic over-achievers, you'll enjoy your career with us!
DISCLAIMER
The preceding job description has been designed to indicate the general nature and level of work performed by employees within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities and qualifications required of employees assigned to the job.
We are an Equal Opportunity Employer and do not discriminate against any employee or applicant for employment because of race, color, sex, age, national origin, religion, sexual orientation, gender identity, status as a veteran, and basis of disability or any other federal, state or local protected class.
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Wind River Systems
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Wind River Systems
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ALAMEDA ALLIANCE FOR HEALTH
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