OverviewAs a Medical Coding Specialist (Chennai, India ~ Office-based)you will be joining the worlds largest & most comprehensive clinical research organisation, powered by healthcare intelligence.ResponsibilitiesWhat you will be doing:Analyze and evaluate clinical data terminology (medical history verbatim, adverse experiences and/or concomitant medications) for coding purposes.Recognize and initiate resolution of data inconsistencies with subsequent follow-up until satisfactory resolution.Ensure medical accuracy, consistency and integrity of the dictionary system by concise coding by thorough term/drug research and definition.Create/maintain ad-hoc computer procedures utilized in generating subset dictionary listings for sponsor review and approval.Demonstrate initiative and ability to work under pressure to organize work requests and set priorities as defined by sponsor driven project milestone deadlines.Write coding SOPs and study specific guidelines.Maintain Clinical Data Management SOPs.Clinical Data Management contact for coding related questions and/or query resolutions.Sponsor contact for study related questions and/or query resolutions.Interact with various Data Management and other functional area colleagues, including, but not limited to: Biostatistics and Programming, Clinical, Project Management, Safety, site personnel, etc.Provide assistance, mentoring, and/or training to Clinical Data Management staff such as Clinical Data Coordinators and/or Data Entry staff, as necessary.Proactively makes recommendations regarding new tools and methodsPossesses expert knowledge of coding applications, databases, processes and tools and serves as a coding liaison for cross functional groups such as Global Patient Safety and Medical Directors.Exercises independent judgment in developing methods, techniques and evaluation criteria for obtaining resultsProactively makes recommendations regarding the development of coding conventions and procedures related to Medical Coding.QualificationsAt least a Bachelors of Nursing or Science, Bachelors of the Arts OR at least 5 years Clinical experience, either in-house or in the fieldMinimum 3-4 years experience in Data ManagementKnowledge, Skills, and Abilities:Knowledge of ICH and GCP guidelinesKnowledge of medical terminology with emphasis on anatomy and physiologyDemonstrate knowledge of the Clinical Trial ProcessDemonstrate knowledge of the Data Management ProcessKnowledge of Drug Development ProcessAbility to think critically and use good problem solving skillsAttention to detailStrong organizational and time management skillsExcellent verbal and written communications skillsKnowledge of the MedDRA and WhoDrug classification dictionariesKnowledge of ClinTrial, SQL, MS Word, Excel, PowerPointWhat ICON can offer you:Our success depends on the quality of our people. Thats why weve made it a priority to build a diverse culture that rewards high performance and nurtures talent.In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.Our benefits examples include:
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