Respond to medical information queries/product quality complaints/general queries that may be received over the telephone call, email, fax etc. Receive information, record, and report Adverse Drug Reaction in timelines. Execute drug safety data management processes – a combination of call intake, call dialogue documentation, peer review, case follow-up. Assume responsibility for quality of data processed.
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As a Clinical Trial Manager you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. You will assume responsibility for an individual project, or many projects and communicate in an optimal way, making sure that specific client objectives are met. Responsible for the set-up and maintenance of the project(s).