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Online Resumes with "WHOdrug"
Registered Nurse - Drug Safety Associate,Coder, Product Surveillance/Product Safety
I am seeking for a stable and well established company that is growing. Also,what I am looking for in a new job is for employers that care about their employees and acknowleges them for their good hard work. I would also hope that good training is provided so that the individual such as myself can be productive for the company and contribute towards it's success rate. I would also hope that it was a warm welcoming environm...
Ideal Companies: Cephalon Pharmaceutical, Teva Pharmaceutical, Azur Pharmaceutical, GlaxoSmithKline, United BioSource
Tags for this Online Resume: Registered Nurse, Drug Safety Associate, Coder, Safety Surveillance, Adverse Event Coordinator
Graduate Student Clinical Research Organization Management
To gain a position at a research institute or pharmaceutical company; which will allow me to utilize the knowledge that I'm currently learning in my clinical research management degree program.
Tags for this Online Resume: RAVE 5.6, CRO contracts, MedRA & WHODRUG, Protocol, Investigator budgets, EPIC & IDX
RN Medical Coder - 18 years experience
Remote Medical Coder experienced in with ICD-9CM, ICD-10, WHODrug, WHO-ART, COSTART and MedDRA coding practices. Knowledge of diseases, drugs, dictionaries, and coding conventions. Multiple compound ownership interfacing with Clinical, Clinical Data Management and Clinical Safety to ensure appropriate coding for report analysis. Responsibilities include the daily running of studies, documentation of all procedures, regular...
Clinical Research
Data Management Clinical Research.
Tags for this Online Resume: Adverse Event Coding, Medical Terminology, Clinical Data Management, WHODRUG coding, Medical Transcriptionist, Medical Chart Review
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
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
Admissions Director - 0 Years of Experience
SUMMARY * Pharmacovigilance Associate with over 2+ years of experience in Drug Safety and Clinical practice fields with clear understanding of EDC (Electronic Data Capture) * Experience in performing successful data management, triage, case entry, MedDRA, WHOdrug dictionaries, narrative writing, peer review, case follow-up, case review and report preparation * Performing Data entry and Quality check adverse event reports fr...
Tags for this Online Resume: Quality, General Practice, HYGIENE, Medical, Surgical, Acceptance Testing, Assessments, Business Intelligence, Coding, Database, healthcare
