Novo Nordisk hiring Associate Medical Coding Professional @ Bangalore

Associate Medical Coding Professional

Category:  Data & AI

Location:  Bangalore, Karnataka, IN

Department: Data Systems & 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.

Key responsibilities:

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:

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 & 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.

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