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– A minimum of 2 years experience in Pharmaceutical industry or in a clinical setting (including experience in hospitals, nursing homes, or clinics);
– Medical coding experience (e.g. therapeutic area knowledge, clinical development or drug safety) – direct experience with MedDRA and WHO-Drug is mandatory;
– Working knowledge of Good Clinical Data Management Practices, ICH Good Clinical Practices, investigational and post marketing regulatory guidelines is preferred;
– Experience with MS Office products;
– Experience in researching information utilizing available resources including publications and the World Wide Web;
– Effective communication, organization and time management skills;
– Ability to work independently under tight time constraints;
– Good interpersonal skills and the ability to operate effectively in an international environment
Last Date:
22nd August, 2014
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