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Online Resumes with "GCP FDA ICH"
Clinical Supply Operation, Edison, NJ - 8+ Years of experience in pharmaceutical R&D, Clinical supply operations. Knowledge and experience in GMP, GCP and FDA/ICH guidelines. Good experience of computer programming and use of MS Suite of Applications, Dat
Proven expertise in managing teams, streamline project paths encompassing an understanding of scientific data, analysis and interpretation of results, clinical developability and commercial viability of projects.
Objectives: To seek a growth opportunity in US pharmaceutical industry, a role in clinical research areas such as Drug Safety/Pharmacovigilance, Medical Writing, and Medical affairs.
Tags for this Online Resume: drug safety, pharmacovigilance, medical writing, clinical research, clinical trial or study, managerial/supervisory experience, senior level in global pharma company, risk management, US work authorization, GCP, FDA, ICH, detail-oriented, results driven, drug , medical , safety, clinical, writing, FDA, GCP, ICH, senior, regulatory, responsible, pharmaceutical