Associate medical coding professional

Department : Data Systems and Automation (DSA), Are you detail:oriented and passionate about ensuring the accuracy and compliance of clinical trial data? Do you have experience in medical coding and data management within the pharmaceutical industry? If so, we have an exciting opportunity for you to join our team as an Associate Medical Coding Professional. The Position As an Associate Medical Coding Professional, your primary responsibility will be to perform timely and accurate categorization of verbatim text in assigned clinical trials to standard medical dictionaries and nomenclature such as MedDRA and WHODrug Global using the TMS Application. You will also be responsible for performing ATC coding on concomitant medications with multiple ATC codes based on project/trial requirements. Additionally, you will ensure compliance with internal and external coding procedures by coordinating with Senior/Medical Coding Professional and Global Safety, and maintain contact with relevant external organizations. Reporting on the status of coding of clinical trials will also be part of your role. Key responsibilities: stylemargin:bottom:2.0px;margin:top:2.0px: : Perform timely and accurate categorization of verbatim text in assigned clinical trials to standard medical dictionaries and nomenclature (MedDRA and WHODrug Global) using the TMS Application : Perform ATC coding on concomitant medications with multiple ATC codes based on project/trial requirements : Ensure compliance with internal and external coding procedures by coordinating with Senior/Medical Coding Professionals and Global Safety, and maintain contact with relevant external organizations : Report on the status of coding of clinical trials Qualifications To be successful in this role, we are looking for candidates with the following qualifications: stylemargin:bottom:2.0px;margin:top:2.0px: : M.Sc / B.Sc in Life Science or comparable degree in medicine, nursing, pharmacy, veterinary science, or clinical information management or equivalent qualifications : Preferably 3 years of data management experience, with the majority of this within the Pharma industry or Development : Preferably knowledge of Medical Coding dictionaries : Preferably experience in project management : Ability and willingness to adjust quickly to new situations in a continuously developing environment : Team:oriented personality with a high degree of flexibility and cross:cultural awareness : Understanding of project management : Knowledge of ICH/GCP and drug development preferable About the department Data Systems and Automation (DSA), Data Management, Bengaluru, is a highly competent and diverse team of professionals responsible for providing functional and system support to execute clinical trials across the Product Development Plan portfolio. The team possesses a strong understanding of Clinical Systems and interfaces, with an end:to:start mindset focused on standardizing data flow across systems. They excel in Electronic Case Report Form (eCRF) development using Central Designer and possess knowledge of Clinical Data Interchange Standards Consortium (CDISC) concepts, including annotated Case Report Form (aCRF), Study Data Tabulation Model (SDTM) mapping, SAS programming, Study Data Review Guideline (SDRG), among others. These skills are crucial for aiding CDISC submission, which is a mandate from regulatory authorities. Working at Novo Nordisk Novo Nordisk is a leading global healthcare company with a 100:year legacy of driving change to defeat serious chronic diseases. Building on our strong legacy within diabetes, we are growing massively and expanding our commitment, reaching millions around the world and impacting more than 40 million patient lives daily. All of this has made us one of the 20 most valuable companies in the world by market cap. Our success relies on the joint potential and coll