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Online Resumes with "WHO Drug"
Clinical Data Manager
Implemented knowledge of ICH GCP and CDISC Standards. Proven organizational skills with the ability to learn quickly; excellent time management, meet tight deadlines; manage multiple tasks and changing priorities while working in a high-pressured environment. Reputable for my attention to detail skills and strong ability to respond and solve problems in real time to fulfill customer expectations. Ability to work effectively...
Tags for this Online Resume: organized, data, bilingual, pharmaceutical, SQL Language, SAS, ClinTrial, ClinAccess, detail oriented
Drug Safety, Home based - 4 years exp - Argus - SAE processing - SUSAR reporrting - Narrative writing - coding using MedDRA & WHO Drug - Workflow management.
Looking for a full time permanent home based/regional position in Drug Safety.
Tags for this Online Resume: Drug Safety, Clinical Safety, Pharmacovigilance
Medical/Clinical Coding Specalist
To secure a rewarding and challenging position in pharmaceutical coding using MedDRA, Who Art, Who Drug, ICD, and other dictionaries utilizing my extensive knowledge and education toward a rewarding career opportunity
Microbiologist - 6 Years of Experience
Qualifications of equipment's. * Analyst qualifications. * On the Job training. * Testing method validation. MAJOR AUDITS FACED: USFDA, TGA, MHRA, ANVISA (Brazil), UKRAINE, GSK, NHL, W.H.O, DRUG CONTROLLER AUDIT. VALIDATION EXPOSURE: * Media fill validation * Antibiotic bio assay * Excel sheet validation for calculations. * Sterility method validation * Bioburden method validation * Microbial Enumeration Test * Bacterial En...
Tags for this Online Resume: Microbiology, Quality, Quality Assurance, Quality Control, Distribution, Test, Training, Audit, Communication Skills, English Language
Pharmacist - 14 Years of Experience - Near 19115
Experienced with Oracle Clinical, ClinTrial, ARGUS 7.0.7 databases, MedDRA 20.0, Who Drug coding systems, and EDC system.
Tags for this Online Resume: Management, Insurance, Managed Care, Coding, Data Entry, Data Management, Documentation, Pharmaceutical, Protocol, Regulatory Affairs
Analysis of patient data through bedside care and pharmaceutical research for 35 years of exemplary work and experience
Objective * RN with 11 years of critical care experience with broad therapeutic clinical experience, expertise in development of processes for patient care, implementation and global training and project oversight. * Sixteen years of clinical research experience, which includes nine years in Drug Safety/Pharmacovigilance experience analyzing subject data. * Quality focused Data Management Associate Director of Clinical List...
Tags for this Online Resume: Business Development, Database, Development Activities, Infrastructure, Gastrointestinal, Intensive Care, Oracle, Critical Care, clinical, research, clinical trials, cro, pharmaceutical, Clinical
Clinical Research - 2 Years of Experience - Near 11418
SUMMARY: * 2 years of experience in the field of clinical data management, producing data review and management objects in various clinical studies and phases in daily bases. * Coding knowledge in MedDRA and WHO Drug systems, Sound knowledge in US FDA and ICH safety reporting advices * Thorough with project set up, quality assurance, data review, data analysis, database clean up and database closing using data management sy...
Tags for this Online Resume: Pricing, Protocol, Research, Data Entry, Data Management, Management, Project Planning, Quality Assurance, Services, Support
Pharmacist - 2 Years of Experience
Familiarity with FDA regulations, standard operating procedures (SOPs), good programming practices (GPP). * Utilized MedDRA and WHO-DRUG dictionaries in creating summary tables for Adverse Events and Concomitant Medications respectively.
Tags for this Online Resume: Information Technology, Coding, Data Migration, Distribution, Documentation, Programming, Project Management, Project Manager, SAP, SAS
Licensed Nurse - 20 Years of Experience - Near 18974
I have extensive experience in writing clinical and regulatory documents in the Pharmaceutical industry which include regulatory and safety I have completed medical encoding (MeDRA), data and quality review management. My past experience included responsibilities for preparing safety sections within key documents such as Investigations Brochure, clinical study reports, writing safety narratives to be included in final stud...
Tags for this Online Resume: Management, Oncology, DS, Query, Medical, Oracle, Oracle Clinical, Database, Encoder, Risk Management
