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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
Lead Project Manager- Clinical Trials
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.
Ideal Companies: Vertex Pharmaceuticals, Amgen Inc., Takeda Pharmaceuticals
drug safety/pharmacovgilance/medical writing-9 years experience-global pharmaceutical
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
