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Regulatory Affairs, Clinical Research, Quality Assurance
A degreed professional with over 4 years of experience in the pharmaceutical/Biotech industry with multi-functional Regulatory, Clinical and Quality background. Demonstrated ability to expand beyond the scope of assigned responsibilities to gain proficiency in new areas. Responsibilities have ranged from managing the preparation, submission of INDs, BLAs, ANDAs/NDA, to reviewing QMS, essential regulatory documents to ensure compliance with GLP, GCP, ICH and GMP regulations. Working Knowledge of PET products.
Admissions Director
About Me
Industry: |
Healthcare & Medical |
|---|---|
Occupation: |
Admissions Director |
Education level: |
Master |
Will Relocate: |
Yes |
Location: |
Upper Marlboro, MD |
