years proven experience in a pharmaceutical regulatory affairs environment including compilation and submission experience of working in several groups in regulatory affairs or experience at a health authority. Implement
years proven experience in a pharmaceutical regulatory affairs environment including compilation and submission experience of working in several groups in regulatory affairs or experience at a health authority. Candidates
or PhD may be an advantage. Experience in regulatory affairs, preferably in human medicines - minimum
Clinical Development and Clinical Operations // Regulatory Affairs // Market Access External // Thought Leaders
Clinical Development and Clinical Operations // Regulatory Affairs // Market Access External // Thought Leaders
experience with training, quality assurance, regulatory affairs, trial management, and CRO liaison
TO
experience with training, quality assurance, regulatory affairs, trial management, and CRO liaison TO APPLY:
experience with training, quality assurance, regulatory affairs, trial management, and CRO liaison TO APPLY: