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Online Resumes with "Formulating source documents"
Clinical Research Coordinator
Profile: Certified Clinical Research Associate professional with extensive recent focus in CVS research and clinical trials. Combine resourcefulness and problem solving skills with clinical knowledge to consistently deliver improved research and production results. Team player dedicated to quality, continuous improvement and bottom-line objectives. QUALIFICATION HIGHLIGHTS • Knowledgeable in all areas of research including...
Ideal Companies: quintiles, Pfizer, Novartis, Aerotek, Abbott, J&J, Merck
Tags for this Online Resume: CRA program, clinical research coordinator
Clinical Pharmacologist (PhD)
A Study Co-ordinator (PhD in Pharmacology) with more than 2.0 year of experience in the pharmaceutical industry. Demonstrated ability to attain and maintain a working knowledge of GCP, schedule Y (Indian CDSCO guidelines), Clinical Trial Document (CTD), and applicable SOPs. Expertise in BA/BE studies, managing clinical trials data, formulating source documents and data collection charts and severe adverse event reporting. C...
Tags for this Online Resume: Clinical Pharmacologist, ClinicalPhamacokinetics, Clinical PK-PD, BABE studies, Phase III studies
